Results 121 to 130 of about 1,167 (171)
Some of the next articles are maybe not open access.
Journal of the American Academy of Dermatology, 1997
Juvenile xanthogranuloma (JXG) is a benign, self-healing disorder characterized by solitary or multiple yellow-red nodules on the skin and, occasionally, in other organs. It is predominantly a disease of infancy or early childhood, although adults may also be affected.
A, Hernandez-Martin +3 more
openaire +2 more sources
Juvenile xanthogranuloma (JXG) is a benign, self-healing disorder characterized by solitary or multiple yellow-red nodules on the skin and, occasionally, in other organs. It is predominantly a disease of infancy or early childhood, although adults may also be affected.
A, Hernandez-Martin +3 more
openaire +2 more sources
Annals of Otology, Rhinology & Laryngology, 1989
The skin of the head and neck is an area of predilection for xanthogranuloma, formerly called nevoxanthoendothelioma. Spontaneous resolution is the usual course for this benign, nonneoplastic lesion that is composed of macrophages and Touton giant cells and occurs principally in infants and children.
openaire +2 more sources
The skin of the head and neck is an area of predilection for xanthogranuloma, formerly called nevoxanthoendothelioma. Spontaneous resolution is the usual course for this benign, nonneoplastic lesion that is composed of macrophages and Touton giant cells and occurs principally in infants and children.
openaire +2 more sources
Journal of Pediatric Ophthalmology & Strabismus, 1982
Juvenile xanthogranuloma (JXG) is a disease of unknown etiology and pathogenesis which was first recognized by dermatologists. The ocular complications provide the primary concern and notably affect the iris, producing spontaneous hemorrhages in the anterior chamber.
R D, Harley, N, Romayananda, G H, Chan
openaire +2 more sources
Juvenile xanthogranuloma (JXG) is a disease of unknown etiology and pathogenesis which was first recognized by dermatologists. The ocular complications provide the primary concern and notably affect the iris, producing spontaneous hemorrhages in the anterior chamber.
R D, Harley, N, Romayananda, G H, Chan
openaire +2 more sources
RETROPERITONEAL XANTHOGRANULOMA
Pediatrics, 1962A second case of a retroperitoneal xanthogranuloma in a child is presented. The tumor is very rare, and its retroperitoneal location is characteristic. The importance of this tumor is its possible relation to the other known histiocytoses, such as eosinophilic granuloma, Hand-Schüller-Christian disease, and Letterer-Siwe disease.
M, KRUGLY +3 more
openaire +2 more sources
Acta Pathologica Japonica, 1985
A 46‐year‐old man with a suspected malignant submucosal tumor received a transabdominoperineal rectal amputation. The histologic diagnosis was xanthogranuloma. The differentiation of xanthogranuloma from malignant fibrous histiocytoma and other histiocytic tumors is difficult in the preoperative stage.
M, Morimatsu +4 more
openaire +2 more sources
A 46‐year‐old man with a suspected malignant submucosal tumor received a transabdominoperineal rectal amputation. The histologic diagnosis was xanthogranuloma. The differentiation of xanthogranuloma from malignant fibrous histiocytoma and other histiocytic tumors is difficult in the preoperative stage.
M, Morimatsu +4 more
openaire +2 more sources
Journal of Pediatric Ophthalmology & Strabismus, 1991
ABSTRACT Three cases of histologically proven limbal xanthogranuloma are presented. All three cases presented with a yellow raised swelling at the limbus and no other ocular or systemic abnormality. A simple excision of the lesion was carried out in all cases and histological examination revealed features typical of xanthogranuloma.
L M, Collum +3 more
openaire +2 more sources
ABSTRACT Three cases of histologically proven limbal xanthogranuloma are presented. All three cases presented with a yellow raised swelling at the limbus and no other ocular or systemic abnormality. A simple excision of the lesion was carried out in all cases and histological examination revealed features typical of xanthogranuloma.
L M, Collum +3 more
openaire +2 more sources
British Journal of Dermatology
Necrobiotic xanthogranuloma is a very rare, histiocytic disease characterized by destructive skin lesions and often arising in the setting of monoclonal gammopathy. A diagnosis of necrobiotic xanthogranuloma is made based on its typical cutaneous features and therefore requires experienced physicians who are familiar with its appearance.
Henning Klapproth +2 more
openaire +2 more sources
Necrobiotic xanthogranuloma is a very rare, histiocytic disease characterized by destructive skin lesions and often arising in the setting of monoclonal gammopathy. A diagnosis of necrobiotic xanthogranuloma is made based on its typical cutaneous features and therefore requires experienced physicians who are familiar with its appearance.
Henning Klapproth +2 more
openaire +2 more sources
Seminars in Cutaneous Medicine and Surgery, 2007
Necrobiotic xanthogranuloma (NXG) is an uncommon granulomatous disease involving the skin and extracutaneous tissues. In its typical clinical presentation, it consists of multiple indurate yellow-brownish plaques or nodules, usually located on the periorbital area.
Jesús, Fernández-Herrera +1 more
openaire +2 more sources
Necrobiotic xanthogranuloma (NXG) is an uncommon granulomatous disease involving the skin and extracutaneous tissues. In its typical clinical presentation, it consists of multiple indurate yellow-brownish plaques or nodules, usually located on the periorbital area.
Jesús, Fernández-Herrera +1 more
openaire +2 more sources
Nonnecrobiotic Necrobiotic Xanthogranuloma
The American Journal of Dermatopathology, 2007N ...
Ferrara G +4 more
openaire +6 more sources
Bilateral Retroperitoneal Xanthogranuloma
British Journal of Urology, 1981Retroperitoneal processes involving the urinary tract are relatively infrequent and include mainly idiopathic retroperitoneal fibrosis or carcinoma‐tous periureteritis. The existence of a retroperitoneal xanthogranuloma leading to bilateral hydro‐nephrosis is exceptional, since only one case has been reported (Sadoughi
Vandendris, Michel +2 more
openaire +3 more sources

