Badr A S, Saadeh C K, Yeary J, Hamous J, Khandheria B
Department of Medicine, Texas Tech University Health Sciences Center, Amarillo, USA.
South Med J. 1997 Mar;90(3):321-4. doi: 10.1097/00007611-199703000-00011.
Dermatomyositis (DM) has been associated with gastrointestinal malignancy but not with polyps or adenoma. We report a case of villous adenoma associated with DM. An 80-year-old white woman was referred for a rash of 2 months' duration that was suggestive of DM. On examination, Gottron's papules and heliotrope rash were seen. Muscle strength was 4/5 in the proximal upper and lower extremities. Despite normal muscle enzyme values, electromyographic and nerve conduction studies were supportive of the diagnosis of DM. DM was confirmed by deltoid muscle biopsy. Heme-positive stool was seen on rectal examination. Colonoscopy revealed a large tubulovillous adenoma in the cecum, which was resected. The patient was given oral prednisone, 60 mg/day. Within 4 weeks after surgery, steroids were tapered to one third the original dose. Within 9 months, steroid therapy had been discontinued with no evidence of disease activity.
皮肌炎(DM)与胃肠道恶性肿瘤有关,但与息肉或腺瘤无关。我们报告一例与DM相关的绒毛状腺瘤病例。一名80岁白人女性因持续2个月的皮疹前来就诊,该皮疹提示为DM。检查时,可见Gottron丘疹和向阳疹。近端上下肢肌力为4/5。尽管肌肉酶值正常,但肌电图和神经传导研究支持DM的诊断。三角肌活检确诊为DM。直肠检查发现大便潜血阳性。结肠镜检查显示盲肠有一个大的管状绒毛状腺瘤,已将其切除。给予患者口服泼尼松,60毫克/天。术后4周内,类固醇逐渐减量至原剂量的三分之一。9个月内,类固醇治疗已停用,无疾病活动迹象。