Schutt-Aine J C, Comeau J C, Sood N, Sinkford S M
J Natl Med Assoc. 1979 Sep;71(9):873-4.
A seven-year, eight-month-old Mexican-American boy was admitted to the hospital with a history of prolonged fever and cervical adenitis. The fever persisted for approximately two weeks and was associated with bilateral conjunctivitis, dryness and redness of the lips, and a deeply red tongue with marked hypertrophy of the papillae. Approximately two weeks following admission a peculiar desquamation of the perianal area was noted, followed by the desquamation of the hands and feet typically noted with mucocutaneous lymph node syndrome (MLNS).Numerous laboratory studies were performed and were not revealing. With the desquamation of the hands and feet a diagnosis of MLNS was believed confirmed. This case is unusual because there was no cutaneous eruption so characteristic of MLNS, and also because of the presence of the peculiar perianal desquamation which has not been previously reported.
一名7岁8个月大的墨西哥裔美国男孩因长期发热和颈部腺炎病史入院。发热持续约两周,伴有双侧结膜炎、嘴唇干燥发红以及舌头深红且乳头明显肥大。入院约两周后,发现肛周区域出现特殊脱皮现象,随后手脚也出现脱皮,这是黏膜皮肤淋巴结综合征(MLNS)的典型表现。进行了多项实验室检查,但均无结果。随着手脚脱皮,MLNS的诊断被认为得到了证实。该病例不同寻常,因为没有MLNS典型的皮肤疹,还因为出现了此前未报道过的特殊肛周脱皮现象。