Kurose N, Nakagawa H, Iozumi K, Nogita T, Furue M, Ishibashi Y
Department of Dermatology, Faculty of Medicine, University of Tokyo, Japan.
J Am Acad Dermatol. 1992 Feb;26(2 Pt 2):359-63. doi: 10.1016/0190-9622(92)70056-l.
A 15-year-old Japanese girl had widespread annular serpiginous erythematous plaques, bilateral granulomatous uveitis, bloody diarrhea, and seronegative arthralgia. She also had anemia and leukopenia. The histopathologic findings were compatible with those of annular elastolytic giant cell granuloma. Elastolytic granulomas were also found in the cervical lymph nodes, terminal ileum, parietal peritoneum, and mesentery. Bilateral hilar lymphadenopathy, hypercalcemia, and an increased level of angiotensin converting enzyme were not observed throughout the clinical course. To the best of our knowledge, systemic elastolytic granulomatosis has not been previously described in annular elastolytic giant cell granuloma or sarcoidosis. This case may represent a type of granulomatosis in the broad spectrum of annular elastolytic giant cell granuloma and sarcoidosis.
一名15岁的日本女孩出现广泛的环状匐行性红斑斑块、双侧肉芽肿性葡萄膜炎、血性腹泻和血清阴性关节痛。她还患有贫血和白细胞减少症。组织病理学检查结果与环状弹性组织溶解性巨细胞肉芽肿相符。在颈部淋巴结、回肠末端、壁层腹膜和肠系膜中也发现了弹性组织溶解性肉芽肿。在整个临床过程中未观察到双侧肺门淋巴结肿大、高钙血症和血管紧张素转换酶水平升高。据我们所知,系统性弹性组织溶解性肉芽肿病此前在环状弹性组织溶解性巨细胞肉芽肿或结节病中尚未有过描述。该病例可能代表了环状弹性组织溶解性巨细胞肉芽肿和结节病广泛谱系中的一种肉芽肿病类型。