Results 131 to 140 of about 4,020 (177)
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Acta Obstetricia et Gynecologica Scandinavica, 1989
A case of intravenous leiomyomatosis is presented along with a review of the literature. The condition is a neoplasia of smooth muscle originating from the uterus, with vermiform extensions into veins. Although histologically benign, the clinical course can be fatal if intravenous tumor progresses to the heart.
P, Konrad, L, Mellblom
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A case of intravenous leiomyomatosis is presented along with a review of the literature. The condition is a neoplasia of smooth muscle originating from the uterus, with vermiform extensions into veins. Although histologically benign, the clinical course can be fatal if intravenous tumor progresses to the heart.
P, Konrad, L, Mellblom
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Vulvar leiomyomatosis in a patient with esophagogastric leiomyomatosis: Review of the syndrome
Gynecologic Oncology, 1991A case of vulvar leiomyomatosis in a young adult with a history of esophagogastrectomy as a child for esophagogastric leiomyomatosis is presented. The steroid receptor profile of the tumor is described. Therapy with a combination of gonadotropin suppression and surgery was undertaken. The literature pertaining to this rare combination is discussed.
K, Faber +3 more
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Diffuse Leiomyomatosis of the Esophagus
Digestive Surgery, 2000<i>Background:</i> Leiomyomas are rare esophagus neoplasms. They are usually solitary, and the diffuse lesion is extremely rare. <i>Case Report:</i> A 19-year-old male presented with a 3-year history of occasional dysphagia and postprandial regurgitation.
Y L, Cheng +4 more
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LEIOMYOMATOSIS PERITONEALIS DISSEMINATA
Acta Obstetricia et Gynecologica Scandinavica, 1981Abstract. Leiomyomatosis peritonealis disseminata (LPD) is a rare disease characterized by the development of multiple subperitoneal leiomyomas, which are widespread in the peritoneal cavity. Of the previously reported LPD cases, nine patients were pregnant, two were on oral contraceptives and one had a granulosa‐cell tumor.
H, Ström, L, Jacobson, K, Hedberg
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Diffuse leiomyomatosis of the esophagus
Digestive Diseases and Sciences, 1980A case of diffuse leiomyomatosis of the esophagus which was successfully resected is presented. The patient was a 44-year-old man who had an abnormal filling defect, which was incidentally discovered during esophagography, and was observed for two years.
T, Kabuto +5 more
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Disseminated peritoneal leiomyomatosis
Virchows Archiv A Pathological Anatomy and Histology, 1977Disseminated peritoneal leiomyomatosis is an unusual condition characterized by the development of numerous nodules in the peritoneal cavity which histologically have the appearance of smooth muscle tumors. The ninth proven case of this ill-understood disorder is presented here, with comments on some of the other published instances.
K, Aterman, G M, Fraser, R H, Lea
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Leiomyomatosis Peritonealis Disseminata
Obstetrics & Gynecology, 1980The ninth documented case of leiomyomatosis peritonealis disseminata (LPD) combined with pregnancy is presented. Light and electron microscopic studies revealed that the smaller tumors were composed partly of decidual cells and partly of fibroblasts, and the larger tumors contained cells resembling smooth muscle cells.
S, Fujii +5 more
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Familial cutaneous leiomyomatosis
Journal of the American Academy of Dermatology, 1981A 24-year-old Caucasian man was evaluated because of a history of multiple firm, reddish, papulonodular skin lesions occurring over the buttocks, thighs, and lower portions of his back and legs since the age of 17 years. Most lesions had developed within 1 year of onset and had become very painful.
H N, Thyresson, W P, Su
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Leiomyomatosis Peritonealis Disseminata
Australian and New Zealand Journal of Obstetrics and Gynaecology, 1978Summary: A case of leiomyomatosis peritonealis disseminata in a 34‐year‐old para 3 is presented.
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Diffuse leiomyomatosis of the uterus
Histopathology, 1995The clinical and pathological features of four cases of the rare entity diffuse leiomyomatosis of the uterus are described. The patients, who ranged in age from 28 to 35 years, presented with a six month to ten year history of abnormal uterine bleeding, dysmenorrhoea and an enlarged uterus.
N J, Mulvany, A G, Ostör, I, Ross
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