Results 211 to 220 of about 34,984 (234)
Some of the next articles are maybe not open access.
Annals of Plastic Surgery, 1987
A cutaneous leiomyosarcoma arose in the upper lip skin of a 22-year-old patient. This unusual tumor was diagnosed clinically as a basal cell carcinoma although histological studies confirmed a leiomyosarcoma. The tumor was excised using Mohs technique and the wound reconstructed with a nasolabial flap and full-thickness skin graft.
J J, Iacobucci +3 more
openaire +2 more sources
A cutaneous leiomyosarcoma arose in the upper lip skin of a 22-year-old patient. This unusual tumor was diagnosed clinically as a basal cell carcinoma although histological studies confirmed a leiomyosarcoma. The tumor was excised using Mohs technique and the wound reconstructed with a nasolabial flap and full-thickness skin graft.
J J, Iacobucci +3 more
openaire +2 more sources
Journal of Surgical Oncology, 1995
AbstractTwo cases of duodenal leiomyosarcoma were encountered, both of which appeared benign by gross and histologic criteria. Both patients suffered recurrences with poor outcomes. We reviewed the literature and found four other such cases and examined the outcomes in the world literature with respect to tumor size and extent of surgical resection ...
T, Fishbein, M, Carroll, R M, Beazley
openaire +2 more sources
AbstractTwo cases of duodenal leiomyosarcoma were encountered, both of which appeared benign by gross and histologic criteria. Both patients suffered recurrences with poor outcomes. We reviewed the literature and found four other such cases and examined the outcomes in the world literature with respect to tumor size and extent of surgical resection ...
T, Fishbein, M, Carroll, R M, Beazley
openaire +2 more sources
Acta Otorrinolaringologica (English Edition), 2007
Laryngeal leiomyosarcoma is a highly infrequent malignancy, with less than fifty reports in the scientific literature world-wide. Diagnosis is based on immunohistochemistry and, occasionally, on electron microscopy techniques, making it difficult to be done preoperatively.
Eduardo, Morera Serna +4 more
openaire +2 more sources
Laryngeal leiomyosarcoma is a highly infrequent malignancy, with less than fifty reports in the scientific literature world-wide. Diagnosis is based on immunohistochemistry and, occasionally, on electron microscopy techniques, making it difficult to be done preoperatively.
Eduardo, Morera Serna +4 more
openaire +2 more sources
Urology, 1981
A case of urachal leiomyosarcoma in a twenty-eight-year-old man is presented. His treatment and a review of the literature are discussed.
D, Noyes, R K, Vinson
openaire +2 more sources
A case of urachal leiomyosarcoma in a twenty-eight-year-old man is presented. His treatment and a review of the literature are discussed.
D, Noyes, R K, Vinson
openaire +2 more sources
Acta Obstetricia et Gynecologica Scandinavica, 1990
A case of leiomyosarcoma of the vulva is presented. Differential diagnostic problems, route of metastasis and treatment are discussed. Radical vulvectomy was performed, with no signs of recurrence or metastasis 30 months after the operation.
Lars Bo Krag Maller +3 more
openaire +2 more sources
A case of leiomyosarcoma of the vulva is presented. Differential diagnostic problems, route of metastasis and treatment are discussed. Radical vulvectomy was performed, with no signs of recurrence or metastasis 30 months after the operation.
Lars Bo Krag Maller +3 more
openaire +2 more sources
The Journal of Laryngology & Otology, 2000
Abstract We report one case of leiomyosarcoma (LMS) of the larynx occurring in a patient with a history of immunosuppressive therapy, and offer a critical review of the literature. Epstein-Barr virus (EBV) genome was not identified in the neoplastic cells. The patient was treated with endoscopic resection and post-operative radiotherapy.
Marioni, G. +5 more
openaire +4 more sources
Abstract We report one case of leiomyosarcoma (LMS) of the larynx occurring in a patient with a history of immunosuppressive therapy, and offer a critical review of the literature. Epstein-Barr virus (EBV) genome was not identified in the neoplastic cells. The patient was treated with endoscopic resection and post-operative radiotherapy.
Marioni, G. +5 more
openaire +4 more sources
Journal of Gastroenterology, 1998
In adults, rectal leiomyosarcoma is uncommon, and anal leiomyosarcoma is even more rare. We report one patient with anal leiomyosarcoma and one patient with a biphasic clinical history, with three occurrences of perineal leiomyosarcomas after surgically resected rectal leiomyoma. We discuss the characteristics of these rare entities based upon a review
T K, Wang, M T, Chung
openaire +2 more sources
In adults, rectal leiomyosarcoma is uncommon, and anal leiomyosarcoma is even more rare. We report one patient with anal leiomyosarcoma and one patient with a biphasic clinical history, with three occurrences of perineal leiomyosarcomas after surgically resected rectal leiomyoma. We discuss the characteristics of these rare entities based upon a review
T K, Wang, M T, Chung
openaire +2 more sources
Journal of the American Academy of Dermatology, 2003
Leiomyosarcoma of the skin is a rare tumor that cannot be diagnosed clinically because its gross appearance is nonspecific. The primary skin tumor usually appears as a solitary nodule. It may arise de novo in the dermis or in the subcutaneous tissue, or as a metastatic lesion from an internal neoplasm.
Julianne H, Kuflik +2 more
openaire +2 more sources
Leiomyosarcoma of the skin is a rare tumor that cannot be diagnosed clinically because its gross appearance is nonspecific. The primary skin tumor usually appears as a solitary nodule. It may arise de novo in the dermis or in the subcutaneous tissue, or as a metastatic lesion from an internal neoplasm.
Julianne H, Kuflik +2 more
openaire +2 more sources
Primary Mediastinal Leiomyosarcoma
The Thoracic and Cardiovascular Surgeon, 1993A 44-year-old woman complaining of thoracic back pain was found to have a large mediastinal leiomyosarcoma. This was completely excised. No adjuvant treatment was given. Follow-up after 24 months showed no evidence of disease. For these rare tumours surgery offers the best treatment, although local recurrence and metastases do occur.
van Schil, Paul +6 more
openaire +3 more sources
Obstetrics & Gynecology, 2000
Uterine myxoid leiomyosarcoma is rare, has a poor prognosis, and must be distinguished from a uterine myoma with myxomatous change.A 56-year-old woman with a history of epigastric pain and generalized abdominal swelling had a peritoneal cavity filled with tumor that originated from the posterior uterine wall.
K, Kasahara +3 more
openaire +2 more sources
Uterine myxoid leiomyosarcoma is rare, has a poor prognosis, and must be distinguished from a uterine myoma with myxomatous change.A 56-year-old woman with a history of epigastric pain and generalized abdominal swelling had a peritoneal cavity filled with tumor that originated from the posterior uterine wall.
K, Kasahara +3 more
openaire +2 more sources