Sporadic lymphangioleiomyomatosis with multiple atypical features: A case report and literature review

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dc.contributor.authorWang, Xen_US
dc.contributor.authorSu, Fen_US
dc.contributor.authorZhou, Fen_US
dc.contributor.authorFeng, Men_US
dc.date.accessioned2020-04-10T01:48:26Z
dc.date.available2020-04-10T01:48:26Z
dc.date.issued2018-03
dc.description.abstractLymphangioleiomyomatosis (LAM) is a rare, genetically determined, progressive interstitial lung disease, which almost exclusively affects women, especially at the childbearing age. The initial symptoms and radiographic changes in a patient with LAM are always associated with the respiratory system. Here, we present a case of mediastinal and abdominal LAM of a 22-year-old male, where LAM cells are negative for human melanoma black-45 ( HMB-45). The report of this uncharacterized LAM case will make a significant contribution to the realization of LAM associated clinical features, diagnostic approaches, and its afterward treatments.en_US
dc.identifier.affiliationsDepartment of Oncology, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, Chinaen_US
dc.identifier.affiliationsDepartment of Oncology, The First Affiliated Hospital of Lanzhou University, Lanzhou, Gansu, Chinaen_US
dc.identifier.citationWang X, Su F, Zhou F, Feng M. Sporadic lymphangioleiomyomatosis with multiple atypical features: A case report and literature review. Indian Journal of Pathology and Microbiology. 2018 Mar; 61(1): 94-97en_US
dc.identifier.issn0377-4929
dc.identifier.issn0974-5130
dc.identifier.placeIndiaen_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/196139
dc.languageenen_US
dc.publisherIndian Association of Pathologists and Microbiologistsen_US
dc.relation.issuenumber1en_US
dc.relation.volume61en_US
dc.source.urihttps://dx.doi.org/10.4103/IJPM.IJPM_843_16en_US
dc.subjectExtrapulmonaryen_US
dc.subjectHMB-45 negativeen_US
dc.subjectlymphangioleiomyomatosisen_US
dc.subjectmanen_US
dc.titleSporadic lymphangioleiomyomatosis with multiple atypical features: A case report and literature reviewen_US
dc.typeJournal Articleen_US
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