Results 131 to 140 of about 4,020 (177)
Some of the next articles are maybe not open access.

Intravenous Leiomyomatosis

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
openaire   +2 more sources

Vulvar leiomyomatosis in a patient with esophagogastric leiomyomatosis: Review of the syndrome

Gynecologic Oncology, 1991
A 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
openaire   +2 more sources

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
openaire   +2 more sources

LEIOMYOMATOSIS PERITONEALIS DISSEMINATA

Acta Obstetricia et Gynecologica Scandinavica, 1981
Abstract. 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
openaire   +2 more sources

Diffuse leiomyomatosis of the esophagus

Digestive Diseases and Sciences, 1980
A 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
openaire   +2 more sources

Disseminated peritoneal leiomyomatosis

Virchows Archiv A Pathological Anatomy and Histology, 1977
Disseminated 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
openaire   +2 more sources

Leiomyomatosis Peritonealis Disseminata

Obstetrics & Gynecology, 1980
The 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
openaire   +2 more sources

Familial cutaneous leiomyomatosis

Journal of the American Academy of Dermatology, 1981
A 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
openaire   +2 more sources

Leiomyomatosis Peritonealis Disseminata

Australian and New Zealand Journal of Obstetrics and Gynaecology, 1978
Summary: A case of leiomyomatosis peritonealis disseminata in a 34‐year‐old para 3 is presented.
openaire   +2 more sources

Diffuse leiomyomatosis of the uterus

Histopathology, 1995
The 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
openaire   +2 more sources

Home - About - Disclaimer - Privacy