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<meta name="keywords" content="C1403035, neoplastic process, subcutaneous lipoma, subcutaneous lipomas, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="The presence of subcutaneous lipoma." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=234674
|
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ConceptID=C1403035
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Subcutaneous lipoma</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>234674</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information."><span class="highlight" style="background-color:">C1403035</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Neoplastic Process</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Subcutaneous lipomas</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Subcutaneous lipoma (762396004)</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
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<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0001031">HP:0001031</a></td></tr>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">The presence of subcutaneous lipoma. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
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</div>
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<div class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="TLline">Subcutaneous lipoma</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/21047" ref="tree=MeSH" title="MedGen record for Pathological Conditions, Signs and Symptoms">Pathological Conditions, Signs and Symptoms</a></span><ul><li><span class="TLline"><a href="/medgen/18325" ref="tree=MeSH" title="MedGen record for Pathological process">Pathological process</a></span><ul><li><span class="TLline"><a href="/medgen/4347" ref="tree=MeSH" title="MedGen record for Disease">Disease</a></span><ul><li><span class="TLline"><a href="/medgen/10294" ref="tree=MeSH" title="MedGen record for Neoplasm">Neoplasm</a></span><ul><li><span class="TLline"><a href="/medgen/10296" ref="tree=MeSH" title="MedGen record for Neoplasm by anatomical site">Neoplasm by anatomical site</a></span><ul><li><span class="TLline"><a href="/medgen/19993" ref="tree=MeSH" title="MedGen record for Neoplasm of the skin">Neoplasm of the skin</a></span><ul><li><span class="matched_ds">Subcutaneous lipoma</span><ul><li><span class="TLline"><a href="/medgen/870393" ref="tree=MeSH" title="MedGen record for Painful subcutaneous lipomas">Painful subcutaneous lipomas</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_112">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_9957"><div><strong>Multiple endocrine neoplasia, type 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>9957</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0025267</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Neoplastic Process</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Multiple endocrine neoplasia type 1 (MEN1) includes varying combinations of more than 20 endocrine and non-endocrine tumors. Endocrine tumors become evident either by overproduction of hormones by the tumor or by growth of the tumor itself. Parathyroid tumors are the most common MEN1-associated endocrinopathy; onset in 90% of individuals is between ages 20 and 25 years with hypercalcemia evident by age 50 years; hypercalcemia causes lethargy, depression, confusion, anorexia, constipation, nausea, vomiting, diuresis, dehydration, hypercalciuria, kidney stones, increased bone resorption/fracture risk, hypertension, and shortened QT interval. Pituitary tumors include prolactinoma (the most common), which manifests as oligomenorrhea/amenorrhea and galactorrhea in females and sexual dysfunction in males. Well-differentiated endocrine tumors of the gastroenteropancreatic (GEP) tract can manifest as Zollinger-Ellison syndrome (gastrinoma); hypoglycemia (insulinoma); hyperglycemia, anorexia, glossitis, anemia, diarrhea, venous thrombosis, and skin rash (glucagonoma); and watery diarrhea, hypokalemia, and achlorhydria syndrome (vasoactive intestinal peptide [VIP]-secreting tumor). Carcinoid tumors are non-hormone-secreting and can manifest as a large mass after age 50 years. Adrenocortical tumors can be associated with primary hypercortisolism or hyperaldosteronism. Non-endocrine tumors include facial angiofibromas, collagenomas, lipomas, meningiomas, ependymomas, and leiomyomas.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/9957">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_140807"><div><strong>Encephalocraniocutaneous lipomatosis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>140807</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0406612</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Encephalocraniocutaneous lipomatosis (ECCL) comprises a spectrum of predominantly congenital anomalies. In its typical form, ECCL is characterized by congenital anomalies of the skin (nevus psiloliparus, patchy or streaky non-scarring alopecia, subcutaneous lipomas in the frontotemporal region, focal skin aplasia or hypoplasia on the scalp, and/or small nodular skin tags on the eyelids or between the outer canthus and tragus), eye (choristoma), and brain (in particular intracranial and spinal lipomas). To a much lesser degree, the bones and the heart can be affected. About 40% of affected individuals have bilateral abnormalities of the skin or the eyes. About one third of affected individuals have normal cognitive development, another one third have mild developmental delay (DD) or intellectual disability (ID), and the final one third have severe or unspecified DD/ID. Half of individuals have seizures. Affected individuals are at an increased (i.e., above the general population) risk of developing brain tumors, particularly low-grade gliomas such as pilocytic astrocytomas. There is evidence that oculoectodermal syndrome (OES) may constitute a clinical spectrum with ECCL, with OES on the mild end and ECCL on the more severe end of the spectrum.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/140807">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_331813"><div><strong>Cerebelloparenchymal Disorder VI</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>331813</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C1834711</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/331813">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_767432"><div><strong>Cowden syndrome 5</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>767432</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C3554518</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">PIK3CA-related overgrowth spectrum (PROS) encompasses a range of clinical findings in which the core features are congenital or early-childhood onset of segmental/focal overgrowth with or without cellular dysplasia. Prior to the identification of PIK3CA as the causative gene, PROS was separated into distinct clinical syndromes based on the tissues and/or organs involved (e.g., MCAP [megalencephaly-capillary malformation] syndrome and CLOVES [congenital lipomatous asymmetric overgrowth of the trunk, lymphatic, capillary, venous, and combined-type vascular malformations, epidermal nevi, skeletal and spinal anomalies] syndrome). The predominant areas of overgrowth include the brain, limbs (including fingers and toes), trunk (including abdomen and chest), and face, all usually in an asymmetric distribution. Generalized brain overgrowth may be accompanied by secondary overgrowth of specific brain structures resulting in ventriculomegaly, a markedly thick corpus callosum, and cerebellar tonsillar ectopia with crowding of the posterior fossa. Vascular malformations may include capillary, venous, and less frequently, arterial or mixed (capillary-lymphatic-venous or arteriovenous) malformations. Lymphatic malformations may be in various locations (internal and/or external) and can cause various clinical issues, including swelling, pain, and occasionally localized bleeding secondary to trauma. Lipomatous overgrowth may occur ipsilateral or contralateral to a vascular malformation, if present. The degree of intellectual disability appears to be mostly related to the presence and severity of seizures, cortical dysplasia (e.g., polymicrogyria), and hydrocephalus. Many children have feeding difficulties that are often multifactorial in nature. Endocrine issues affect a small number of individuals and most commonly include hypoglycemia (largely hypoinsulinemic hypoketotic hypoglycemia), hypothyroidism, and growth hormone deficiency.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/767432">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_767433"><div><strong>Cowden syndrome 6</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>767433</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C3554519</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The features of Cowden syndrome overlap with those of another disorder called Bannayan-Riley-Ruvalcaba syndrome. People with Bannayan-Riley-Ruvalcaba syndrome also develop hamartomas and other noncancerous tumors. Some people with Cowden syndrome have relatives diagnosed with Bannayan-Riley-Ruvalcaba syndrome, and other affected individuals have the characteristic features of both conditions. Based on these similarities, researchers have proposed that Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome represent a spectrum of overlapping features known as PTEN hamartoma tumor syndrome (named for the genetic cause of the conditions) instead of two distinct conditions.\n\n\n\nSome people do not meet the strict criteria for a clinical diagnosis of Cowden syndrome, but they have some of the characteristic features of the condition, particularly the cancers. These individuals are often described as having Cowden-like syndrome. Both Cowden syndrome and Cowden-like syndrome are caused by mutations in the same genes.\n\nCowden syndrome is associated with an increased risk of developing several types of cancer, particularly cancers of the breast, a gland in the lower neck called the thyroid, and the lining of the uterus (the endometrium). Other cancers that have been identified in people with Cowden syndrome include kidney cancer, colorectal cancer, and an agressive form of skin cancer called melanoma. Compared with the general population, people with Cowden syndrome develop these cancers at younger ages, often beginning in their thirties or forties. People with Cowden syndrome are also more likely to develop more than one cancer during their lifetimes compared to the general population. Other diseases of the breast, thyroid, and endometrium are also common in Cowden syndrome. Additional signs and symptoms can include an enlarged head (macrocephaly) and a rare, noncancerous brain tumor called Lhermitte-Duclos disease. A small percentage of affected individuals have delayed development, intellectual disability, or autism spectrum disorder, which can affect communication and social interaction.\n\nAlmost everyone with Cowden syndrome develops hamartomas. These growths are most commonly found on the skin and mucous membranes (such as the lining of the mouth and nose), but they can also occur in the intestine and other parts of the body. The growth of hamartomas on the skin and mucous membranes typically becomes apparent by a person's late twenties.\n\nCowden syndrome is a genetic disorder characterized by multiple noncancerous, tumor-like growths called hamartomas and an increased risk of developing certain cancers.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/767433">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_331813" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cerebelloparenchymal Disorder VI</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_767432" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cowden syndrome 5</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_767433" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cowden syndrome 6</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_140807" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Encephalocraniocutaneous lipomatosis</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_9957" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Multiple endocrine neoplasia, type 1</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35125438">Deoxycholic Acid Injection in the Management of Difficult-to-Remove Subcutaneous Lipomas.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sutaria A,
|
||
Kapoor A,
|
||
Sharma YK,
|
||
Gupta A</span><br />
|
||
<span class="medgenPMjournal">Dermatol Surg</span>
|
||
2022 Mar 1;48(3):367-368.
|
||
doi: 10.1097/DSS.0000000000003343.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35125438" target="_blank">35125438</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30001658">Prenatal diagnosis of closed spina bifida: multicenter case series and review of the literature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Milani HJF,
|
||
Barreto EQS,
|
||
Chau H,
|
||
To NH,
|
||
Moron AF,
|
||
Meagher S,
|
||
Da Silva Costa F,
|
||
Araujo Júnior E</span><br />
|
||
<span class="medgenPMjournal">J Matern Fetal Neonatal Med</span>
|
||
2020 Mar;33(5):736-742.
|
||
Epub 2018 Sep 6
|
||
doi: 10.1080/14767058.2018.1500543.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30001658" target="_blank">30001658</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10343959">Differential diagnosis of cutaneous and subcutaneous tumours assessed by 7.5 MHz ultrasonography.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ulrich J,
|
||
Gollnick H</span><br />
|
||
<span class="medgenPMjournal">J Eur Acad Dermatol Venereol</span>
|
||
1999 Mar;12(2):187-9.
|
||
doi: 10.1111/j.1468-3083.1999.tb01020.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10343959" target="_blank">10343959</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(subcutaneous%20lipoma)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (15)</a></div></div>
|
||
</div>
|
||
<div class="display-none help-popup" id="guidelinesHelpPM">These guidelines are articles in PubMed that match specific search criteria developed by MedGen to capture the most relevant practice guidelines. This list may not be comprehensive and may include broader topics as well. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div><div class="display-none help-popup" id="guidelinesHelpCurated">These guidelines are manually curated by the MedGen team
|
||
to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
|
||
<div class="portlet mgSection" id="ID_103">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_clinical_studies">Recent clinical studies</h1><a sid="103" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">Etiology</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/32530476">Corpus Callosum Lipomas in Children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gezer B,
|
||
Karabagli H,
|
||
Koktekir E,
|
||
Sahinoglu M,
|
||
Karabagli P</span><br />
|
||
<span class="medgenPMjournal">Turk Neurosurg</span>
|
||
2020;30(4):573-576.
|
||
doi: 10.5137/1019-5149.JTN.27692-19.6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32530476" target="_blank">32530476</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22743947">Gone in 30 seconds: a quick and simple technique for subcutaneous lipoma removal.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rao SS,
|
||
Davison SP</span><br />
|
||
<span class="medgenPMjournal">Plast Reconstr Surg</span>
|
||
2012 Jul;130(1):236e-238e.
|
||
doi: 10.1097/PRS.0b013e3182550439.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22743947" target="_blank">22743947</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15326839">Xanthelasma and lipoma in Leonardo da Vinci's Mona Lisa.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dequeker J,
|
||
Muls E,
|
||
Leenders K</span><br />
|
||
<span class="medgenPMjournal">Isr Med Assoc J</span>
|
||
2004 Aug;6(8):505-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15326839" target="_blank">15326839</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9500386">Posttraumatic lipomas: where do they really come from?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Signorini M,
|
||
Campiglio GL</span><br />
|
||
<span class="medgenPMjournal">Plast Reconstr Surg</span>
|
||
1998 Mar;101(3):699-705.
|
||
doi: 10.1097/00006534-199803000-00017.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9500386" target="_blank">9500386</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8178644">Lipomyelomeningocele: a 9-year review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shian WJ,
|
||
Chi CS,
|
||
Wong TT</span><br />
|
||
<span class="medgenPMjournal">Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi</span>
|
||
1994 Jan-Feb;35(1):57-62.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8178644" target="_blank">8178644</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Subcutaneous%20lipoma%22%20AND%20Etiology%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (24)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/26802948">Endoscopic resection of subcutaneous lipoma and tumor-like lesion of the foot.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lui TH</span><br />
|
||
<span class="medgenPMjournal">Foot (Edinb)</span>
|
||
2016 Mar;26:36-40.
|
||
Epub 2015 Sep 9
|
||
doi: 10.1016/j.foot.2015.09.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26802948" target="_blank">26802948</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22743947">Gone in 30 seconds: a quick and simple technique for subcutaneous lipoma removal.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rao SS,
|
||
Davison SP</span><br />
|
||
<span class="medgenPMjournal">Plast Reconstr Surg</span>
|
||
2012 Jul;130(1):236e-238e.
|
||
doi: 10.1097/PRS.0b013e3182550439.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22743947" target="_blank">22743947</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22211431">Osteochondrolipoma: a subcutaneous lipoma with chondroid and bone differentiation of the chest wall.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gru AA,
|
||
Santa Cruz DJ</span><br />
|
||
<span class="medgenPMjournal">J Cutan Pathol</span>
|
||
2012 Apr;39(4):461-3.
|
||
Epub 2011 Dec 29
|
||
doi: 10.1111/j.1600-0560.2011.01855.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22211431" target="_blank">22211431</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21519959">Report of two cases of subcutaneous lipoma over the finger and review of literature: case series: benign tumour.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gupta A,
|
||
Singal R,
|
||
Mittal A,
|
||
Goyal M</span><br />
|
||
<span class="medgenPMjournal">Musculoskelet Surg</span>
|
||
2011 Dec;95(3):247-9.
|
||
Epub 2011 Apr 26
|
||
doi: 10.1007/s12306-011-0134-7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21519959" target="_blank">21519959</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3665587">Palmar subcutaneous lipoma.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kaminsky CA,
|
||
de Kaminsky AR,
|
||
Chajchir A,
|
||
Costantini S</span><br />
|
||
<span class="medgenPMjournal">Cutis</span>
|
||
1987 Jul;40(1):29-32.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3665587" target="_blank">3665587</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Subcutaneous%20lipoma%22%20AND%20Diagnosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (42)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/26598562">Ectopic Schistosoma mansoni Eggs Inside a Lipoma.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sabino KR,
|
||
Nunes MB,
|
||
Petroianu A</span><br />
|
||
<span class="medgenPMjournal">Am J Trop Med Hyg</span>
|
||
2016 Jan;94(1):156-7.
|
||
Epub 2015 Nov 23
|
||
doi: 10.4269/ajtmh.15-0287.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26598562" target="_blank">26598562</a><a href="/pmc/articles/PMC4710421" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25291347">Increased Prevalence of Subcutaneous Lipomas in Patients With Wilson Disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Schaefer M,
|
||
Gotthardt DN,
|
||
Didion C,
|
||
Stremmel W,
|
||
Weiss KH</span><br />
|
||
<span class="medgenPMjournal">J Clin Gastroenterol</span>
|
||
2015 Aug;49(7):e61-3.
|
||
doi: 10.1097/MCG.0000000000000248.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25291347" target="_blank">25291347</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22885708">The role of flexible hollow core carbon dioxide lasers in resection of lumbar intraspinal lipomas.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Desai SK,
|
||
Paulson D,
|
||
Thompson BJ,
|
||
Patterson J,
|
||
Mohanty A</span><br />
|
||
<span class="medgenPMjournal">Childs Nerv Syst</span>
|
||
2012 Oct;28(10):1785-90.
|
||
Epub 2012 Aug 12
|
||
doi: 10.1007/s00381-012-1884-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22885708" target="_blank">22885708</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22647077">Haematogenous abdominal wall metastasis of differentiated, alpha-fetoprotein-negative hepatocellular carcinoma after previous antiandrogen therapy within a site of lipoma manifestation since childhood.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zachau L,
|
||
Zeckey C,
|
||
Schlue J,
|
||
Sander J,
|
||
Meyer-Heithuis C,
|
||
Winkler M,
|
||
Klempnauer J,
|
||
Schrem H</span><br />
|
||
<span class="medgenPMjournal">World J Surg Oncol</span>
|
||
2012 May 30;10:98.
|
||
doi: 10.1186/1477-7819-10-98.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22647077" target="_blank">22647077</a><a href="/pmc/articles/PMC3408335" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Subcutaneous%20lipoma%22%20AND%20Therapy%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (4)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/32530476">Corpus Callosum Lipomas in Children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gezer B,
|
||
Karabagli H,
|
||
Koktekir E,
|
||
Sahinoglu M,
|
||
Karabagli P</span><br />
|
||
<span class="medgenPMjournal">Turk Neurosurg</span>
|
||
2020;30(4):573-576.
|
||
doi: 10.5137/1019-5149.JTN.27692-19.6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32530476" target="_blank">32530476</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22743947">Gone in 30 seconds: a quick and simple technique for subcutaneous lipoma removal.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rao SS,
|
||
Davison SP</span><br />
|
||
<span class="medgenPMjournal">Plast Reconstr Surg</span>
|
||
2012 Jul;130(1):236e-238e.
|
||
doi: 10.1097/PRS.0b013e3182550439.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22743947" target="_blank">22743947</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/19802890">Subcutaneous lipoma compressing the common peroneal nerve and causing palsy: sonographic diagnosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hsu YC,
|
||
Shih YY,
|
||
Gao HW,
|
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Huang GS</span><br />
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<span class="medgenPMjournal">J Clin Ultrasound</span>
|
||
2010 Feb;38(2):97-9.
|
||
doi: 10.1002/jcu.20643.
|
||
<span class="bold">PMID: </span><a href="/pubmed/19802890" target="_blank">19802890</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15722612">Parietal lipomeningocele--case report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yamashita S,
|
||
Kunishio K,
|
||
Tamiya T,
|
||
Nakamura T,
|
||
Ogawa D,
|
||
Igawa HH,
|
||
Kuroda Y,
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Nagao S</span><br />
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<span class="medgenPMjournal">Neurol Med Chir (Tokyo)</span>
|
||
2005 Feb;45(2):112-5.
|
||
doi: 10.2176/nmc.45.112.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15722612" target="_blank">15722612</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9500386">Posttraumatic lipomas: where do they really come from?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Signorini M,
|
||
Campiglio GL</span><br />
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<span class="medgenPMjournal">Plast Reconstr Surg</span>
|
||
1998 Mar;101(3):699-705.
|
||
doi: 10.1097/00006534-199803000-00017.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9500386" target="_blank">9500386</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Subcutaneous%20lipoma%22%20AND%20Prognosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (17)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/32530476">Corpus Callosum Lipomas in Children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gezer B,
|
||
Karabagli H,
|
||
Koktekir E,
|
||
Sahinoglu M,
|
||
Karabagli P</span><br />
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||
<span class="medgenPMjournal">Turk Neurosurg</span>
|
||
2020;30(4):573-576.
|
||
doi: 10.5137/1019-5149.JTN.27692-19.6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32530476" target="_blank">32530476</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31280360">CT and MR imaging findings of solitary nevus lipomatosus cutaneous superficialis: radiological-pathological correlation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kawaguchi M,
|
||
Kato H,
|
||
Tomita H,
|
||
Hara A,
|
||
Matsuo M</span><br />
|
||
<span class="medgenPMjournal">Skeletal Radiol</span>
|
||
2020 Jan;49(1):129-135.
|
||
Epub 2019 Jul 7
|
||
doi: 10.1007/s00256-019-03269-y.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31280360" target="_blank">31280360</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29975963">Bony and Cartilaginous Tissues in Lumbosacral Lipomas.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shimogawa T,
|
||
Morioka T,
|
||
Murakami N,
|
||
Mukae N,
|
||
Hashiguchi K,
|
||
Suzuki SO,
|
||
Iihara K</span><br />
|
||
<span class="medgenPMjournal">Pediatr Neurosurg</span>
|
||
2018;53(5):305-310.
|
||
Epub 2018 Jul 4
|
||
doi: 10.1159/000490391.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29975963" target="_blank">29975963</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15154619">Well-differentiated liposarcoma associated with benign lipoma.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hatano H,
|
||
Morita T,
|
||
Ogose A,
|
||
Hotta T,
|
||
Kobayashi H,
|
||
Honma K</span><br />
|
||
<span class="medgenPMjournal">Anticancer Res</span>
|
||
2004 Mar-Apr;24(2C):1039-44.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15154619" target="_blank">15154619</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10885206">Spinal lipomatous malformations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jindal A,
|
||
Mahapatra AK</span><br />
|
||
<span class="medgenPMjournal">Indian J Pediatr</span>
|
||
2000 May;67(5):342-6.
|
||
doi: 10.1007/BF02820684.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10885206" target="_blank">10885206</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Subcutaneous%20lipoma%22%20AND%20Clinical%20prediction%20guides%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (11)</a></div></div>
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