用于朱文生纤维癌细胞的诊所并分类

P. Reifferscheid, P. Schweizer, G. Müller, A. Flach, Dr. A. Flach, Chirurgischen Univ.-Klinik, Tübingen, Kinderkrankenhaus auf der Bult, Hannover
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引用次数: 0

摘要

从1963年到1983年,共有24例婴儿和儿童(平均年龄3.2岁)因腹外硬纤维瘤样纤维瘤病(F)接受手术治疗。患者按En::illger和Wciss(1983)分类。14名儿童表现为婴儿或少年F, 3名为数字F, 7名为大肠杆菌F。局部切除后病变复发50例(\\)。37.5%有二次局部复发,16.6%超过2次(最多7次)局部复发。F的治疗包括肿瘤的局部根治性切除。局部照射或局部给药皮质类固醇在特殊情况下可能有帮助,如全身给药化疗、皮质类固醇或cAM p抑制剂可能有帮助。
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Zur Klinik und Klassifikation der juvenilen Fibromatosen
From 1963 through 198324 infants and children (mean age 3.2 years) were operated on for extra-abdominal desmoid fi bromatosis (F). The patients were classified according to En ::illger and Wciss (1983). 14 children presented with infantile or juvenile F, 3 with digital F, and 7 with F colli. The lesion recurred after local excision in 50(\\) of the patients. 37.5% had a second local recurrence, and 16.6 % more than 2 (up to 7) local recurrences. Therapy of F consists of radical local excislOn of the tumour. Local irradiation or local administra tion ofcorticosteroids may be helpful in special cases, as may be systemic administration of chemotherapy, corticosteroids or inhibitors of cAM P. Spontaneous regression of F has been observed.
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