López-Estebaranz J L, Rodriguez-Peralto J L, Ortiz Romero P L, Vanaclocha F, Iglesias Díez L
Department of Dermatology, Hospital 12 de Octubre, Madrid, Spain.
J Am Acad Dermatol. 1994 Nov;31(5 Pt 2):897-900. doi: 10.1016/s0190-9622(94)70255-1.
We describe a 40-year-old white man with a peculiar skin eruption in association with polyclonal hypergammaglobulinemia. No underlying disease was detected. A skin biopsy specimen showed a proliferation of mature plasma cells intermingled with some lymphocytes and histiocytes, an appearance consistent with cutaneous plasmacytosis. This disease had been previously described only in Japanese patients. In our patient the disease progressed slowly. Lymph node infiltration by mature plasma cells was later noted.
我们描述了一名40岁的白人男性,其患有一种特殊的皮肤疹,伴有多克隆高球蛋白血症。未检测到潜在疾病。皮肤活检标本显示成熟浆细胞增生,混有一些淋巴细胞和组织细胞,这一表现符合皮肤浆细胞增多症。这种疾病此前仅在日本患者中被描述过。在我们的患者中,疾病进展缓慢。后来发现有成熟浆细胞浸润淋巴结。