LES TUMEURS BRUNES : UN DIAGNOSTIC A EVOQUER EN PATHOLOGIE OSSEUSE MAXILLO-FACIALE
-
Published:2022-12-01
Issue:
Volume:
Page:15-18
-
ISSN:
-
Container-title:INDIAN JOURNAL OF APPLIED RESEARCH
-
language:en
-
Short-container-title:IJAR
Author:
M'Fa SK.1, Bakhil A.1, Buckat H. Buckat1, Hafidi N. El1, Benbachir A.1, Ribag Y.1, Sabani H.1, Khalfi L.1, Hamama J.2, Khatib K. El1
Affiliation:
1. Department of Stomatology and Maxillofacial Surgery, Mohammed V Military Hospital, Mohammed V University, Rabat, Morocco. 2. Department of Stomatology and Maxillofacial Surgery, Mohammed V Military Hospital, Mohammed V University, Rabat, Morocco
Abstract
Brown tumors are a rare non-neoplastic lesion of late onset, resulting from an abnormality of bone metabolism during
hyperparathyroidism. Their localization in the facial skeleton is rare. The positive diagnosis is based on a beam of
arguments and conditions the management; the treatment depends on the etiology. We report a unicentric retrospective descriptive study,
including 4 patients, carried out in the department of oral and maxillofacial surgery of the Mohammed V armed forces hospital in Rabat, over a
15-year period, from January 2007 to January 2022. According to the inclusion criteria, 04 patients were recruited in our study, all female, aged
between 19 and 41 years, with no family history. Mandibular location was found in one patient, maxillary location in two patients, and maxillomandibular location in one patient. Primary hyperparathyroidism on parathyroid adenoma was found in 2 cases, secondary hyperparathyroidism
on chronic renal failure in 1 case and tertiary hyperparathyroidism in 1 case. The treatment of the tumor was surgical in 2 cases (one tumor
removal and one conservative surgical management) and medical in 2 cases. Two patients beneted from a parathyroidectomy. A complete
regression was observed in 75% of cases. This study shows the importance of evoking the diagnosis of a brown tumor in the facial skeleton when
a patient presenting hyperparathyroidism with giant cells on histological examination shows the presence of bone call points, even if they are rare
and/or late. Management is multidisciplinary. Surgical removal is indicated in case of failure of medical treatment, absence or delay of tumor
regression after parathyroidectomy, and will depend on the volume of the localization and the impact of the tumor. It would therefore be
judicious, in the case of a giant cell tumor of the facial skeleton, to establish algorithms allowing a rapid and precise diagnosis guaranteeing an
adequate management.
Publisher
World Wide Journals
Subject
Mechanical Engineering,General Engineering,Religious studies,Communication,Strategy and Management,Communication,Business and International Management,Economics and Econometrics,Communication,Philosophy,Communication,Law,Communication,Communication,Education,Applied Psychology,Communication,Social Psychology,Biomedical Engineering,General Medicine
Reference44 articles.
1. Panagopoulos et al. Osteolytic lesions (brown tumors) of primary hyperparathyroidism misdiagnosed as multifocal giant cell tumor of the distal ulna and radius: a case report. Journal of Medical Case Reports (2018) 12:176 https://doi.org/10.1186/s13256-018-1723-y 2. Bankole et al. Tumeurs brunes osseuses : un diagnostic à ne pas méconnaître. La Revue de Médecine Interne. 2020. https://doi.org/10.1016/j.revmed.2020.10.268 3. Hamdi W, Kaffel D, Ferjani H, Maatallah K, Riahi H, Kchir MM. Tumeurs brunes multiples révélant un adénome parathyroïdien : A propos de deux cas. La tunisie médicale – 2019 ; Vol 97 (n°01) 4. Suheil A, Abdalla B, Mustafa Y, Zaher A. Maxillary and Frontal Bone Simultaneously Involved in Brown Tumor due to Secondary Hyperparathyroidism in a Hemodialysis Patient. Case Rep Oncol Med 2013; 2013:909150. 5. Pradhuman V, Kanika G,Dinesh V, Nitin. Craniofacial brown tumor as a result of secondary hyperparathyroidism in chronic renal disease patient: A rare entity. J Oral Maxillofac Pathol 2014;18(2):267–270.
|
|