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Acquired Perforating Dermatosis Associated with Hodgkin Lymphoma: Rare Associated Manifestation

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dc.contributor.author Ravion Assavanatenapa en_US
dc.contributor.author Supapat Laodheerasiri en_US
dc.date.accessioned 2026-05-15T09:22:11Z
dc.date.available 2026-05-15T09:22:11Z
dc.date.issued 2026-05-15
dc.identifier.citation GMS Medicine Journal. Vol.6, No.2 (May - August 2026) : p.117-122 en_US
dc.identifier.issn 2730-3446
dc.identifier.uri http://mfuir.mfu.ac.th:80/xmlui/handle/123456789/1719
dc.description บทความ (Article) en_US
dc.description.abstract Acquired 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.iso en en_US
dc.publisher School of Medicine, Mae Fah Luang University en_US
dc.subject acquired perforating dermatosis en_US
dc.subject central keratotic plug en_US
dc.subject significant weight loss en_US
dc.subject Hodgkin lymphoma en_US
dc.title Acquired Perforating Dermatosis Associated with Hodgkin Lymphoma: Rare Associated Manifestation en_US
dc.type Article en_US


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