Results 161 to 170 of about 22,944 (232)
Some of the next articles are maybe not open access.
The Journal of Laryngology & Otology, 1999
AbstractFibromatosis represents a diverse group of fibroproliferative tumours. Their behaviour and pathological qualities are situated in an intermediate position between benign and malignant disease. The following represents the pathological and radiological presentation of a 29-year-old female with fibromatosis.
A, Yoskovitch +4 more
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AbstractFibromatosis represents a diverse group of fibroproliferative tumours. Their behaviour and pathological qualities are situated in an intermediate position between benign and malignant disease. The following represents the pathological and radiological presentation of a 29-year-old female with fibromatosis.
A, Yoskovitch +4 more
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Desmoid-type fibromatosis: toward a holistic management
Current Opinion in Oncology, 2021Supplemental Digital Content is available in the text Purpose of review Desmoid-type fibromatosis, a rare locally aggressive fibroblastic proliferation, is a treatment challenge.
N. Penel +2 more
semanticscholar +1 more source
Neurosurgery, 1991
Abstract Fibromatoses are uncommon infiltrative lesions affecting musculoaponeurotic structures, most often of the limbs and trunk. Lesions involving the cranial cavity are rare and require the same aggressive surgical management as elsewhere in the body. This case illustrates their clinical and neuroradiological features and underscores
A, Mitchell +3 more
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Abstract Fibromatoses are uncommon infiltrative lesions affecting musculoaponeurotic structures, most often of the limbs and trunk. Lesions involving the cranial cavity are rare and require the same aggressive surgical management as elsewhere in the body. This case illustrates their clinical and neuroradiological features and underscores
A, Mitchell +3 more
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The American Journal of Surgical Pathology, 1979
Two cases of fibromatosis of the female mammary gland treated by local excision and with a follow-up of 11 and 3 years, respectively, are described. Fibromatosis confined to the breast and not involving the underlying fibroaponeurotic fascia is a rare lesion. Among the handful of cases reported in the literature, diagnostic errors are known to have led
M, Ali, A O, Fayemi, E V, Braun, R, Remy
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Two cases of fibromatosis of the female mammary gland treated by local excision and with a follow-up of 11 and 3 years, respectively, are described. Fibromatosis confined to the breast and not involving the underlying fibroaponeurotic fascia is a rare lesion. Among the handful of cases reported in the literature, diagnostic errors are known to have led
M, Ali, A O, Fayemi, E V, Braun, R, Remy
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Fibromatosis of the mesoappendix
Pathology International, 2000Mesenchymal tumors of the appendix are very rare. Mesenteric fibromatosis is the most common diagnosis in the case of isolated proliferative fibroblastic lesion found in this region. However, the differential diagnosis between fibromatosis and well‐differentiated fibrosarcoma (Grade I) can be difficult in some borderline cases.
M, Pilichowska +4 more
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The Journal of Laryngology & Otology, 1999
AbstractA case of infantile fibromatosis involving the cheek of a three-year-old Sudanese girl is described. The tumour was resected through a sublabial approach.
W M, Janahi +3 more
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AbstractA case of infantile fibromatosis involving the cheek of a three-year-old Sudanese girl is described. The tumour was resected through a sublabial approach.
W M, Janahi +3 more
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European Journal of Pediatric Surgery, 1998
Two rare cases of mesenteric fibromatosis are presented. The first patient had a right upper quadrant mass and colicky abdominal pain. The tumor originated from the mesentery of the colon and it infiltrated the gallbladder, cystic duct, and the liver. The second patient had severe hematemesis and melena.
H, Sarihan +4 more
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Two rare cases of mesenteric fibromatosis are presented. The first patient had a right upper quadrant mass and colicky abdominal pain. The tumor originated from the mesentery of the colon and it infiltrated the gallbladder, cystic duct, and the liver. The second patient had severe hematemesis and melena.
H, Sarihan +4 more
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Japanese Journal of Clinical Oncology, 2020
OBJECTIVE The treatment modality for desmoid-type fibromatosis has shifted from surgery to conservative treatment. The guideline committee for clinical care of extra-abdominal desmoid-type fibromatosis in Japan conducted a systematic review of treatment ...
Koki Shimizu +4 more
semanticscholar +1 more source
OBJECTIVE The treatment modality for desmoid-type fibromatosis has shifted from surgery to conservative treatment. The guideline committee for clinical care of extra-abdominal desmoid-type fibromatosis in Japan conducted a systematic review of treatment ...
Koki Shimizu +4 more
semanticscholar +1 more source
American Journal of Roentgenology, 2009
This article illustrates the imaging findings that have pathologic correlation and the clinical presentation of mammary fibromatosis.Mammary fibromatosis is a rare, benign, nonmetastasizing stromal tumor. It presents clinically and radiologically as a palpable, spiculated, and locally invasive tumor that is suspicious for malignancy.
Katrina N, Glazebrook, Carol A, Reynolds
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This article illustrates the imaging findings that have pathologic correlation and the clinical presentation of mammary fibromatosis.Mammary fibromatosis is a rare, benign, nonmetastasizing stromal tumor. It presents clinically and radiologically as a palpable, spiculated, and locally invasive tumor that is suspicious for malignancy.
Katrina N, Glazebrook, Carol A, Reynolds
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Annals of Otology, Rhinology & Laryngology, 1979
Juvenile fibromatosis is a benign lesion with locally aggressive characteristics. Wide surgical excision is the treatment of choice. Radiation therapy can be used for inoperable cases or as adjunctive therapy. Steroid therapy has not been used extensively and deserves further evaluation.
W T, Morioka, V C, Heath, R W, Cantrell
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Juvenile fibromatosis is a benign lesion with locally aggressive characteristics. Wide surgical excision is the treatment of choice. Radiation therapy can be used for inoperable cases or as adjunctive therapy. Steroid therapy has not been used extensively and deserves further evaluation.
W T, Morioka, V C, Heath, R W, Cantrell
openaire +2 more sources