Results 211 to 220 of about 8,801 (261)
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Intravascular angiomatosis

Oral Surgery, Oral Medicine, Oral Pathology, 1978
For 55 years much has been written about a peculiar benign intravascular process which can be misdiagnosed as angiosarcoma unless careful attention is paid by the pathologist to its benign cellular morphology and growth pattern. The cases reported in the literature demonstrate an increased incidence in the extremities and the head and neck, with a ...
K D, McClatchey   +2 more
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Angiomatosis Osteohypotrophica

Scandinavian Journal of Plastic and Reconstructive Surgery, 1982
Based on a clinical and radiological study of seven patients, a syndrome consisting of congenital hemangiomas with arteriovenous fistulae engaging the soft tissues and the bones, and associated with shortening of the involved extremity, for which we suggest the name angiomatosis osteohypotrophica, is reported.
I A, Niechajev, S, Karlsson
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Meningio-angiomatosis

Pathology - Research and Practice, 1989
A case is described of a boy five years old who suffered from left-sided muscular weakness since the first months of life and from absences since the second year of life. He died of valproate-induced hepatic insufficiency. Autopsy of the brain revealed meningio-angiomatosis, a rare but rather benign disorder usually characterized by narrow ...
W, Paulus   +3 more
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Orbitofacial Angiomatosis

Archives of Ophthalmology, 1979
Two patients with orbital vascular malformation ipsilateral facial nevus flammeus were studied. The literature contains one similar case that interestingly shares with our cases the lack of leptomeningeal angiomatosis. Orbitofacial angiomatosis seems to be a distinct entity from meningofacial angiomatosis because of its true vascular malformation of ...
A J, Hofeldt   +4 more
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Diffuse dermal angiomatosis

Journal of Cutaneous Pathology, 2004
Abstract:  Diffuse dermal angiomatosis (DDA) is an acquired, benign vascular proliferation characterized clinically by poorly circumscribed, violaceous, livedoid plaques with frequent ulceration. Histologically, a diffuse interstitial proliferation of CD31‐positive endothelial cells is present within the papillary and reticular dermis.
Bradley K, Draper, Alan S, Boyd
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Sturge-Weber angiomatosis

The Lancet, 2011
A 20-year-old woman presented with a 1-month history of swollen gums. Her medical history included seizures for the past 19 years and a macular patch on the right side of her face since birth. She was taking phenytoin for her seizures. Intraoral examination showed extension of the macular patch on the right side of the oral cavity and generalised ...
Atul P, Sattur, Megha, Goyal
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Cutaneous bacillary angiomatosis

The Indian Journal of Pediatrics, 2002
Bacillary angiomatosis is characterized by unique vascular lesions caused by infection with a small Gram staining bacillus of the genus Bartonella. It usually occurs in immunocompromised persons but can also occur in immunocompetent persons. We report a case of cutaneous bacillary angiomatosis in a 5-year-old immunocompetent child.
Mohammed, Asharaf, S, Letha
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Cryoglobulinaemia and angiomatosis*

British Journal of Dermatology, 1983
A 61-year-old woman is presented with essential cryoglobulinaemia and a 25-year history of recurrent ulceration of the lower legs. She developed multiple benign angiomatous nodules on the face, earlobes and neck. Histologically, they simulated an angiosarcoma and are therefore of considerable diagnostic importance.
J I, Harper, W, Gray, E, Wilson-Jones
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Systemic cystic angiomatosis

The American Journal of Medicine, 1964
Abstract A case of cystic angiomatosis is reported, and twelve similar cases with multicentric skeletal involvement collected from the literature are reviewed. The basic pathologic lesion consists of cysts of either blood or lymph channels. The classification of this disorder is discussed as it relates to either a congenital maldevelopment of vessels ...
S G, SECKLER, H, RUBIN, J G, RABINOWITZ
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AIDS-Related Angiomatosis

The American Journal of Dermatopathology, 1989
We report multifocal cutaneous and mucosal vascular proliferations with the clinical and histological features of lobular capillary hemangioma and histiocytoid hemangioma in a 32-year-old acquired immunodeficiency syndrome patient. The lesions resolved subsequent to erythromycin therapy.
C A, Axiotis   +3 more
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