Results 171 to 180 of about 10,048 (219)
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Urology, 1987
A primary intrascrotal mass clinically mimicking a testicular tumor was found to be a desmoid tumor originating from the spermatic cord. To our knowledge, this is the first reported case of a paratesticular desmoid tumor.
R W, Gluck, G, Bloiso, J, Glasser
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A primary intrascrotal mass clinically mimicking a testicular tumor was found to be a desmoid tumor originating from the spermatic cord. To our knowledge, this is the first reported case of a paratesticular desmoid tumor.
R W, Gluck, G, Bloiso, J, Glasser
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Musculoskeletal Desmoid Tumors
Journal of the American Academy of Orthopaedic Surgeons, 2008Desmoid tumors are benign tumors that exhibit varying degrees of local aggressiveness and diverse growth patterns. Magnetic resonance imaging remains the modality of choice for assessment of the nature and size of the soft-tissue lesion and involvement of surrounding structures.
Harish S, Hosalkar +5 more
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Desmoid tumours of the extremities
International Orthopaedics, 1988The authors report seven cases of desmoid tumors of the extremities. A tumour less than a few centimetres in size is best removed by wide local excision. Large growths should also be excised, but efforts should be made to preserve the vessels and nerves, since malignant transformation and metastases do not occur.
T, Vizkelety, M, Szendröi
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American Journal of Roentgenology, 2011
The purpose of this article is to illustrate the common locations of desmoid tumors (deep fibromatosis), complications of intra- and extraabdominal desmoids, and treatment-related changes in their imaging appearance.Desmoids are locally aggressive fibrous tumors with a tendency to recur.
Atul B, Shinagare +6 more
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The purpose of this article is to illustrate the common locations of desmoid tumors (deep fibromatosis), complications of intra- and extraabdominal desmoids, and treatment-related changes in their imaging appearance.Desmoids are locally aggressive fibrous tumors with a tendency to recur.
Atul B, Shinagare +6 more
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The management of desmoid tumors
International Journal of Radiation Oncology*Biology*Physics, 1992To determine the efficacy of different treatment modalities for desmoid tumors.We reviewed the treatment of 40 patients with histologically confirmed desmoid tumors seen at Duke University Medical Center between 1974 and 1990.Radiotherapy was administered to 16 patients (Group I)--14 with recurrent disease s/p surgery and in two as initial treatment ...
J C, Acker, E H, Bossen, E C, Halperin
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Desmoid fibromatosis of the breast
BMJ Case ReportsDesmoid-type fibromatosis (DTF) is a rare non-metastatic mesenchymal tumour that accounts for only 0.2% of all primary breast neoplasms. This locally aggressive tumour has a high recurrence rate and primarily affects women aged 20–40 years. DTF often presents with features mimicking breast carcinoma, posing diagnostic challenges and the risk of ...
Aqsa Amjad +3 more
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Clinical Radiology, 2015
Desmoid-type fibromatosis is a rare, locally infiltrative, mesenchymal neoplasm that is associated with high rates of local recurrence but lacks the potential to metastasise. The disease affects younger individuals, with a peak age of 30 years, and is the most common cause of an anterior abdominal wall mass in young women of childbearing age.
S, Otero +6 more
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Desmoid-type fibromatosis is a rare, locally infiltrative, mesenchymal neoplasm that is associated with high rates of local recurrence but lacks the potential to metastasise. The disease affects younger individuals, with a peak age of 30 years, and is the most common cause of an anterior abdominal wall mass in young women of childbearing age.
S, Otero +6 more
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Journal of Hand Surgery, 1999
We report a case of a 3-year-old child with a desmoid tumour of the hand, which is an exceedingly rare location. Desmoid tumours of the hand are difficult to treat because of the many important structures concentrated in the area as well as the infiltrative and recurrent character of these tumours.
F, Duteille, G, Dautel, D, Sommelet
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We report a case of a 3-year-old child with a desmoid tumour of the hand, which is an exceedingly rare location. Desmoid tumours of the hand are difficult to treat because of the many important structures concentrated in the area as well as the infiltrative and recurrent character of these tumours.
F, Duteille, G, Dautel, D, Sommelet
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Rozhledy v chirurgii : mesicnik Ceskoslovenske chirurgicke spolecnosti, 2001
The author presents the case-record of a patient with familial adenomatous polyposis and a subsequent large desmoid of the abdominal wall, a review of the symptomatology, and treatment.
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The author presents the case-record of a patient with familial adenomatous polyposis and a subsequent large desmoid of the abdominal wall, a review of the symptomatology, and treatment.
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