[Extra-abdominal desmoid tumors. Therapeutic indications. Apropos of 28 cases]. 1991

P A Chatelard, and F N Gilly, and J P Carret, and J L Vauzelle, and M Brunat, and G Braillon, and H Dejour
Service de Chirurgie Générale et Vasculaire, Centre Hospitalier Lyon Sud, Pierre Bénite, France.

Between 1965 and 1989, 46 desmoid tumors were observed in the hospitals of Lyon. Twenty-eight patients with an extra-abdominal tumor, with a follow-up of at least 6 months were observed. In this group, there were 12 males and 16 females with an average of 26.7 years. Surgical treatment was performed in 26 cases (in one case no treatment was given and in another case isolated chemotherapy was given). In 21 cases (80%) a recurrence of the tumor was seen after the first excision, incomplete in 6 cases. The highest rate of recurrence was seen in the neck, the girdles and the lower limbs; at the end of our review, 9 patients still had a tumor. No primary amputation were performed but two late amputations, one of which was major, were necessary. One tumor evolved into a sarcoma and in another case, lung metastases were seen. Associated radiotherapy was given in 9 cases with resolution in 55%. Tamoxifen was used in 5 cases with stabilization of the tumor. The risk of recurrence was higher in males (p = 0.0147). Age less than 30 years, and incomplete removal of the tumor were the other predictive factors for recurrence (the difference was not significant).

UI MeSH Term Description Entries
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D009362 Neoplasm Metastasis The transfer of a neoplasm from one organ or part of the body to another remote from the primary site. Metastase,Metastasis,Metastases, Neoplasm,Metastasis, Neoplasm,Neoplasm Metastases,Metastases
D009364 Neoplasm Recurrence, Local The local recurrence of a neoplasm following treatment. It arises from microscopic cells of the original neoplasm that have escaped therapeutic intervention and later become clinically visible at the original site. Local Neoplasm Recurrence,Local Neoplasm Recurrences,Locoregional Neoplasm Recurrence,Neoplasm Recurrence, Locoregional,Neoplasm Recurrences, Local,Recurrence, Local Neoplasm,Recurrence, Locoregional Neoplasm,Recurrences, Local Neoplasm,Locoregional Neoplasm Recurrences,Neoplasm Recurrences, Locoregional,Recurrences, Locoregional Neoplasm
D002471 Cell Transformation, Neoplastic Cell changes manifested by escape from control mechanisms, increased growth potential, alterations in the cell surface, karyotypic abnormalities, morphological and biochemical deviations from the norm, and other attributes conferring the ability to invade, metastasize, and kill. Neoplastic Transformation, Cell,Neoplastic Cell Transformation,Transformation, Neoplastic Cell,Tumorigenic Transformation,Cell Neoplastic Transformation,Cell Neoplastic Transformations,Cell Transformations, Neoplastic,Neoplastic Cell Transformations,Neoplastic Transformations, Cell,Transformation, Cell Neoplastic,Transformation, Tumorigenic,Transformations, Cell Neoplastic,Transformations, Neoplastic Cell,Transformations, Tumorigenic,Tumorigenic Transformations
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D003131 Combined Modality Therapy The treatment of a disease or condition by several different means simultaneously or sequentially. Chemoimmunotherapy, RADIOIMMUNOTHERAPY, chemoradiotherapy, cryochemotherapy, and SALVAGE THERAPY are seen most frequently, but their combinations with each other and surgery are also used. Multimodal Treatment,Therapy, Combined Modality,Combined Modality Therapies,Modality Therapies, Combined,Modality Therapy, Combined,Multimodal Treatments,Therapies, Combined Modality,Treatment, Multimodal,Treatments, Multimodal
D005260 Female Females
D005350 Fibroma A benign tumor of fibrous or fully developed connective tissue. Fibromatosis,Fibromyxoma,Myxofibroma,Fibromas,Fibromatoses,Fibromyxomas,Myxofibromas

Related Publications

P A Chatelard, and F N Gilly, and J P Carret, and J L Vauzelle, and M Brunat, and G Braillon, and H Dejour
February 1961, Archives of pathology,
P A Chatelard, and F N Gilly, and J P Carret, and J L Vauzelle, and M Brunat, and G Braillon, and H Dejour
April 1969, Archives of surgery (Chicago, Ill. : 1960),
P A Chatelard, and F N Gilly, and J P Carret, and J L Vauzelle, and M Brunat, and G Braillon, and H Dejour
February 1986, Acta orthopaedica Scandinavica,
P A Chatelard, and F N Gilly, and J P Carret, and J L Vauzelle, and M Brunat, and G Braillon, and H Dejour
December 1984, The Journal of bone and joint surgery. American volume,
P A Chatelard, and F N Gilly, and J P Carret, and J L Vauzelle, and M Brunat, and G Braillon, and H Dejour
January 1955, Gazeta medica portuguesa,
P A Chatelard, and F N Gilly, and J P Carret, and J L Vauzelle, and M Brunat, and G Braillon, and H Dejour
February 1980, Tumori,
P A Chatelard, and F N Gilly, and J P Carret, and J L Vauzelle, and M Brunat, and G Braillon, and H Dejour
October 2010, Journal of surgical oncology,
P A Chatelard, and F N Gilly, and J P Carret, and J L Vauzelle, and M Brunat, and G Braillon, and H Dejour
April 1986, Journal de chirurgie,
P A Chatelard, and F N Gilly, and J P Carret, and J L Vauzelle, and M Brunat, and G Braillon, and H Dejour
December 1985, Revista espanola de las enfermedades del aparato digestivo,
P A Chatelard, and F N Gilly, and J P Carret, and J L Vauzelle, and M Brunat, and G Braillon, and H Dejour
January 1969, Arkhiv patologii,
Copied contents to your clipboard!