Olsen E A, Crawford J R, Vollmer R T
Division of Dermatology, Duke University Medical Center, Durham, NC 27710.
J Am Acad Dermatol. 1988 Jun;18(6):1322-32. doi: 10.1016/s0190-9622(88)70142-5.
A report of a patient with the rare syndrome of sinus histiocytosis with massive lymphadenopathy is presented here. This patient is unusual in several respects, including his longevity after diagnosis, the presence of a benign monoclonal gammopathy, and the characterization of his cutaneous infiltrates by immunofluorescent monoclonal antibody markers. A review of the literature on sinus histiocytosis with massive lymphadenopathy, with particular emphasis on cutaneous manifestations, is given.
本文报道了一例患有罕见的伴巨大淋巴结病的窦性组织细胞增多症综合征的患者。该患者在几个方面表现出不同寻常之处，包括诊断后的长寿、存在良性单克隆丙种球蛋白病以及通过免疫荧光单克隆抗体标志物对其皮肤浸润进行的特征描述。本文对伴巨大淋巴结病的窦性组织细胞增多症的文献进行了综述，特别强调了皮肤表现。
