Results 221 to 230 of about 13,125 (269)
Some of the next articles are maybe not open access.

Pelvic Lipomatosis

British Journal of Urology, 1991
Pelvic lipomatosis is a rare disease in Caucasians. We describe a patient who presented originally with bladder outlet obstruction and later developed vesicoureteric obstruction.
B J, Jones, M R, Butler
openaire   +2 more sources

Encephalocraniocutaneous lipomatosis

Journal of Child Neurology, 1987
Encephalocraniocutaneous lipomatosis is a distinct clinical syndrome characterized by unilateral cerebral malformations and ipsilateral scalp, face, and eye lesions. The cutaneous lesions are confined to the head. The central nervous system lesions consist in part of cerebral hemiatrophy, porencephaly, and defective opercularization of the insula. The
openaire   +2 more sources

Congenital infiltrating lipomatosis of the face with lingual mucosal neuromas associated with a PIK3CA mutation

Pediatric dermatology, 2020
We report the case of a 5‐year‐old girl with congenital right‐sided facial hemihypertrophy and right hemi‐macroglossia with lingual mucosal neuromas. The segmental presentation of findings suggested the diagnosis of congenital infiltrating lipomatosis of
C. Briand   +6 more
semanticscholar   +1 more source

Encephalocraniocutaneous lipomatosis

2015
Encephalocraniocutaneous lipomatosis (ECCL) is an unusual condition marked by characteristic dermatologic and neurologic findings presenting in a mosaic fashion. These are now being found to be due to specific genetic mutations. Traditionally, the diagnostic features include ocular dermoids, scalp changes, and spinal lipomas.
Moise L, Levy, Catherine, Massey
openaire   +2 more sources

Pelvic lipomatosis

Urology, 1976
Three cases of pelvic lipomatosis are presented. Excretory urogram revealed characteristic elevation and elongation of urinary bladder base and relative hyperlucency of pelvic cavity. Associated varying degrees of hydronephrosis and hydroureters are seen secondary to distal ureteral obstruction.
S, Radinsky, E, Cabal, J, Shields
openaire   +4 more sources

Encephalocraniocutaneous Lipomatosis

Journal of Cutaneous Medicine and Surgery: Incorporating Medical and Surgical Dermatology, 2003
Background: Encephalocraniocutaneous lipomatosis (ECCL) is a relatively new, nonhereditary, but congenital, neurocutaneous syndrome with unilateral cutaneous tumors and ipsilateral ophthalmologic and neurologic malformations. The syndrome is rare, with only 25 cases reported since first communication in 1970.
Julita, Gawel   +2 more
openaire   +2 more sources

Mediastinal Lipomatosis

Southern Medical Journal, 1998
Mediastinal lipomatosis is a benign condition characterized by a large amount of mature adipose tissue within the mediastinum. It widens the mediastinum and may simulate mass lesions, thus leading to diagnostic errors. We describe a new case of a huge mediastinal lipomatosis and review 36 cases previously reported in the literature. Computed tomography
K Q, Nguyên   +3 more
openaire   +2 more sources

Adult-Onset Asymmetrical Lipomatosis: Thigh Girdle Lipomatosis

Obesity Surgery, 2020
We present the case of an elderly Caucasian woman with asymmetric lipomatosis of the thigh. Lipomatosis is an exaggerated and widespread growth of mature adipose tissue, infiltrating the surrounding tissues (e.g., muscle). Numerous forms of lipomatosis have been identified: the symmetrical form is the most frequent.
Ceolin C., Busetto L., Sergi G., Enzi G.
openaire   +2 more sources

Mediastinal Lipomatosis

Journal of the Association of Physicians of India
Mediastinal lipomatosis is a benign condition characterized by excessive deposition of unencapsulated mature adipose tissue in the mediastinum.1 The exact prevalence is not known. The available literature mainly consists of some case series and a bunch of case reports.
Ananda, Datta, Raghavendrun, Sivasankar
openaire   +2 more sources

Encephalocraniocutaneous Lipomatosis

Pediatrics, 1978
Two patients with encephalocraniocutaneous lipomatosis have been studied. The main features of the syndrome are unilateral cutaneous and ophthalmologic lesions with ipsilateral cerebral malformations. Seizures beginning in infancy and varying degrees of mental retardation are present in affected patients.
M A, Fishman, C S, Chang, J E, Miller
openaire   +2 more sources

Home - About - Disclaimer - Privacy