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一名患有乳糜泻和IgA缺乏症的女孩患纤维肉瘤。

Fibrosarcoma in a girl with celiac disease and IgA deficiency.

作者信息

Verkasalo M, Savilahti E, Rapola J, Wallgren E I

出版信息

J Pediatr Gastroenterol Nutr. 1985 Oct;4(5):839-41. doi: 10.1097/00005176-198510000-00028.

Abstract

A case of abdominal wall fibrosarcoma in a 17-year-old girl with celiac disease and IgA deficiency is described. Celiac disease was putatively diagnosed with intestinal biopsy at the age of 15 years when she came for hospital investigations because of IgA deficiency and recurrent respiratory infections. The tumor occurred at the age of 17 years during the gluten challenge performed for final diagnosis of celiac disease. Surgical excision, irradiation, and chemotherapy were initially successful. After 7 months, however, the tumor recurred. Reoperation and a new course of irradiation therapy coinciding with the reinstitution of a gluten-free diet proved to be effective in tumor eradication. Nine years after the cessation of cancer treatment she is well and has two healthy children.

摘要

本文描述了一名17岁患有腹腔疾病和IgA缺乏症的女孩患腹壁纤维肉瘤的病例。该女孩15岁时因IgA缺乏症和反复呼吸道感染前来医院检查,经肠道活检初步诊断为腹腔疾病。肿瘤发生在17岁,当时正在进行麸质激发试验以最终确诊腹腔疾病。手术切除、放疗和化疗最初取得了成功。然而,7个月后肿瘤复发。再次手术以及与重新采用无麸质饮食同时进行的新一轮放射治疗被证明对根除肿瘤有效。癌症治疗停止九年后,她身体状况良好,并有两个健康的孩子。

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