Syringolymphoid hyperplasia with alopecia
- 1 January 1984
- journal article
- case report
- Published by Oxford University Press (OUP) in British Journal of Dermatology
- Vol. 110 (1) , 95-101
- https://doi.org/10.1111/j.1365-2133.1984.tb07318.x
Abstract
A 26-year-old man presented with an unusual skin lesion consisting of a hairless area on the left leg studded with reddish-brown papules, together with follicular hyperkeratosis and circumscribed anhidrosis. Skin biopsies showed dense lymphocytic infiltrates in the dermis and around hyperplastic sweat ducts and glands. Similar clinical and histological features have been described in two previous case reports. We propose the term syringolymphoid hyperplasia with alopecia for this unusual skin disease.Keywords
This publication has 10 references indexed in Scilit:
- Cutaneous lymphomatoid granulomatosisClinical and Experimental Dermatology, 1982
- Cutaneous manifestations of lymphomatoid granulomatosis. Report of 44 cases and a review of the literatureArchives of Dermatology, 1981
- Distribution of T cell subsets in human lymph nodes.The Journal of Experimental Medicine, 1981
- Lymphomatoid granulomatosis.A clinicopathologic study of 152 casesCancer, 1979
- Lymphomatoid granulomatosis preceded by chronic granulomatous dermatitisArchives of Dermatology, 1978
- Lymphomatoid granulomatosisClinical and Experimental Dermatology, 1976
- Lymphomatoid GranulomatosisProceedings of the Royal Society of Medicine, 1975
- Lymphomatoid granulomatosis of the skin: Light microscopic and ultrastructural studiesCancer, 1974
- Lymphomatoid granulomatosisPublished by Elsevier ,1972