Please use this identifier to cite or link to this item: http://mfuir.mfu.ac.th:80/xmlui/handle/123456789/1719
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dc.contributor.authorRavion Assavanatenapaen_US
dc.contributor.authorSupapat Laodheerasirien_US
dc.date.accessioned2026-05-15T09:22:11Z-
dc.date.available2026-05-15T09:22:11Z-
dc.date.issued2026-05-15-
dc.identifier.citationGMS Medicine Journal. Vol.6, No.2 (May - August 2026) : p.117-122en_US
dc.identifier.issn2730-3446-
dc.identifier.urihttp://mfuir.mfu.ac.th:80/xmlui/handle/123456789/1719-
dc.descriptionบทความ (Article)en_US
dc.description.abstractAcquired reactive perforating collagenosis (ARPC) is a rare subtype of acquired perforating dermatosis (APD) that typically occurs in adults, often associated with diabetes mellitus or chronic renal failure. However, ARPC has also been reported in association with malignancies and other systemic disorders. We presented the case of a 21-year-old Thai woman presented with multiple erythematous, pruritic papules with central keratotic plugs on the trunk, back, and extremities for five months. With history of chronic cough and significant weight loss of 10 kg over three months. Punch biopsy consistent with ARPC. Further investigations revealed an anterior mediastinal mass, multiple enlarged cervical and intraabdominal lymph nodes, and tiny pulmonary nodules with peribronchovascular consolidations at anterior segment of RUL; concerning for lymphatic or lung involvement. EBUS-guided biopsy showed atypical cells compatible with Classic Hodgkin lymphoma. The patient was diagnosed with ARPC with Hodgkin lymphoma stage IIIB with bulky disease, IPS 0. This case highlights the importance of recognizing ARPC as a potential cutaneous manifestation of underlying malignancy.en_US
dc.language.isoenen_US
dc.publisherSchool of Medicine, Mae Fah Luang Universityen_US
dc.subjectacquired perforating dermatosisen_US
dc.subjectcentral keratotic plugen_US
dc.subjectsignificant weight lossen_US
dc.subjectHodgkin lymphomaen_US
dc.titleAcquired Perforating Dermatosis Associated with Hodgkin Lymphoma: Rare Associated Manifestationen_US
dc.typeArticleen_US
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