Jih D M, Werth V P
Department of Dermatology, University of Pennsylvania, and Philadelphia V.A. Hospital, 19104, USA.
J Am Acad Dermatol. 1998 Aug;39(2 Pt 2):349-51. doi: 10.1016/s0190-9622(98)70387-1.
Low dose methotrexate (MTX) can cause numerous gastrointestinal, pulmonary, central nervous system, and hematologic toxicities. Risk factors include folate deficiency, decreased renal function, older age, increased mean corpuscular volume or concomitant use of trimethoprim-sulphamethoxazole, probenecid, or nonsteroidal antiinflammatory drugs (NSAIDs). We describe a case of isolated thrombocytopenia after a single oral dose of MTX in a 36-year-old woman with sarcoidosis. She had rheumatoid arthritis and her only other medications included NSAIDs. One week after her first oral dose of 7.5 mg MTX, diffuse petechiae developed on her chest, abdomen, and extremities; she had a platelet count of 25,000/mm3. Nine days after discontinuation of both MTX and the NSAID, her platelet count increased to 189,000/mm3.
低剂量甲氨蝶呤(MTX)可导致多种胃肠道、肺部、中枢神经系统和血液学毒性。危险因素包括叶酸缺乏、肾功能下降、年龄较大、平均红细胞体积增加或同时使用甲氧苄啶-磺胺甲恶唑、丙磺舒或非甾体抗炎药(NSAIDs)。我们描述了一例36岁结节病女性单次口服MTX后出现孤立性血小板减少症的病例。她患有类风湿关节炎,唯一的其他药物包括NSAIDs。在首次口服7.5mg MTX一周后,她的胸部、腹部和四肢出现弥漫性瘀点;血小板计数为25,000/mm³。在停用MTX和NSAIDs九天后,她的血小板计数增至189,000/mm³。