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本病较为罕见,国内外报导不多,其病因及发病机制迄今仍未明确。作者于1961年秋诊断1例此病,伴发颈淋巴腺结核。经抗结核药物治疗后,随访观察近二年,未再复发。本文谨将此例报告并就其病因及发病机制试加讨论。病例摘要患者郝某,男性,29岁,(住院号114264)于1961年8月14日入院。患者于六年前春季发病,两下肢出现散在皮下小结节,结节表面皮肤略红肿,颇疼,两下肢运动稍受限制。皮下结节反复发作,每逢病犯时伴有发热,症状
The disease is relatively rare, few reports at home and abroad, the etiology and pathogenesis has not yet clear. The author diagnosed the disease in the autumn of 1961, accompanied by cervical lymph node tuberculosis. After anti-TB drug treatment, follow-up observation of nearly two years, no recurrence. This article would like to report this case and its etiology and pathogenesis try to discuss. Case summary Hao Mou, male, 29 years old, (hospital number 114264) was admitted on August 14, 1961. Patients in the spring six years of onset, two lower extremity scattered subcutaneous nodules, nodular surface of the skin slightly red and swollen, very painful, slightly limited movement of both lower extremities. Subcutaneous nodules recurrent, whenever the disease associated with fever, symptoms