A case of ichthyosiform sarcoidosis with unusual localization

Central European Journal of Medicine - Tập 4 - Trang 388-390 - 2009
Salim Basol Tekin1, Kerim Cayir1, Mehmet Bilici1, Sare Şipal2, Mustafa Atasoy3, Mehmet Türkeli1
1Division of Medical Oncology, Department of Internal Medicine, Erzurum, Turkey
2Department of Pathology, Atatürk University, School of Medicine, Erzurum, Turkey
3Department of Dermatology, Erzurum, Turkey

Tóm tắt

Sarcoidosis is a systemic granulomatous disease of unknown cause that commonly involves the lungs, lymph nodes, bones, liver, spleen, or skin. Cutaneous findings of sarcoidosis occur in 20% to 35% of patients with systemic disease. The recognition of cutaneous lesions is important, because it gives important clues to diagnosis and also allows for easy biopsy. We report a 71-year-old Turkish woman with erythematous lesions, which included widespread, erythematous macules of various sizes on the chest, abdomen, and back on both sides of her body. Fine white scales covered some of the lesions. Hepatomegaly and bilateral hilar lymphadenopathy were also observed. Biopsy specimens of the skin showed dermal, noncaseating, epitheloid granulomas. The diagnosis, based on correlation of the clinical presentation and histopathological findings, was ichthyosiform sarcoidosis with systemic involvement. The difference between our case and other cases of ichthyosiform sarcoidosis described in the literature is that ours involved only the trunk and not the extremities. We are presenting this case because it is an interesting and rare variant of ichthyosiform sarcoidosis.

Tài liệu tham khảo

Kerdel FA., Moschella SL., Sarcoidosis: an updated rewiew, J. Am. Acad. Dermatol., 1984, 11,1–19 Mountcastle ME., Lupton GP., An Ichthyosiform Euption on the Legs, Arch. Dermatol, 1989, 125(10), 1415–1416, 1419 Lupton JR., Figueroa P., Berberian BJ et al., Can granuloma annulare evolve into cutaneus sacoidosis? Cutis., 2000,66(5),390–392 Cather JC., Cohen PR., Ichthyosiform sarcoidosis, J. Am. Acad. Dermatol., 1999, 40(5 pt 2), 862–865 Bense-Kupin L., Pelachyk JM., Ichthyosiform sarcoidosis, Report of two cases and rewiew of the literature, J. Am. Acad. Dermatol., 1987, 17(4),616–620 Matarasso SL., Bruce S., Ichthyosiform sarcoidosis: report of a case, Cutis., 1991, 47(6),405–408 Paller AS., Roenigk AH Jr., Caro WA., Extensive ichthyosiform sarcoidosis in a patient with juvenile rheumatoid arthritis, Arch. Dermatol., 1985,121(2), 171–172 Mallory SB., Paller AS., Ginsburg BC., et al., Sarcoidosis in children: differentiation from juvenile rheumatoid arthritis, Pediatr. Dermatol., 1987, 4(4),313–319 Feind-Koopmans AG., Lucker GP., van de Kerkhof PC., Acquired ichthyosiform erythroderma and sarcoidosis, J. Am. Acad. Dermatol., 1996, 35(5 pt 2),826–828 Kauh YC., Goody HE., Luscombe HA., Ichthyosiform sarcoidosis, Arch. Dermatol. 1978, 114 (1), 100–101 Mora RG., Gullung WH., Sarcoidosis: a case with unusual manifestations, South. Med. J., 1980, 73(8),1063–1065 Matsuoka LY., LeVine M., Glasser S., et al., Ichthyosiform sarcoid, Cutis.,1980, 25(2), 188–189