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[Maxillary brown tumor revealing primary hyperparathyroidism: apropos of a case and review of the literature].
Pan Afr Med J
September 2013
Service d'ORL et chirurgie Cervico-faciale, hôpital 20 Aout, CHU Ibn Rochd, Casablanca, Morocco.
[Primary hyperparathyroidism presenting as a brown tumor of the maxilla and hard palate. Apropos of a case].
Rev Stomatol Chir Maxillofac
April 2001
Service d'ORL et de Chirurgie Maxillo-Faciale, Hôpital des Spécialités, CHU Avicenne, Rabat, Maroc.
Significant controversy persists in the classification of giant cell lesions of the maxillofacial skeleton. Multifocal giant cell lesions are strongly suggestive of hyperparathyroidism brown tumors. Maxillary localization is extremely rare.
View Article and Find Full Text PDF[Microdeletion 22q11: apropos of case of schizophrenia in an adolescent].
Encephale
June 2001
Service de Psychopathologie de l'Enfant et de l'Adolescent, CHU Pitié-Salpêtrière, 47, boulevard de l'Hôpital, 75013 Paris.
Deletion of chromosome 22q11 concerns nearly 1/5.000 births, and is the most frequent interstitial microdeletion. The deletion generates various phenotypes which were initially regarded as distinct syndromes.
View Article and Find Full Text PDF[Surgery for primary hyperparathyroidism in 1998. Apropos of 66 patients and 3 methods of approach].
Ann Chir
May 2000
Service de chirurgie, hôpital de l'Antiquaille, Lyon, France.
Study Aim: The aim of this prospective study was to assess the advantages and disadvantages of cervicotomy, selective lateral approach and video-assisted surgery in the treatment of primary hyperparathyroidism (HPT 1).
Patients And Methods: During 1998, 66 patients were operated on for HPT 1 in the same center. There were 48 women and 18 men (mean age: 58 years, range: 21-84), familial HPT 1 or MEN1 excluded.
[Parathyroid cysts: comments apropos a case].
Ann Ital Chir
December 1999
I Istituto di Clinica Chirurgica, Università degli Studi di Roma La Sapienza.
A case of non-functioning parathyroid cyst is reported, in which the preoperative diagnosis was missed. A careful review of the pertinent literature allows to outline the correct approach to this rare pathology as for the diagnosis and the treatment; as well, to enlight the current controversies about the physiopathology and the pathology.
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