Cherubism in sub-saharan Africa: a first case-report in a child
Cherubism is rare disease and has been rarely reported in African pediatric population. We report here the case of a 10-year-old child who was referred to our hospital for bilateral jaws swelling. Physical examination revealed bilateral swelling symmetry of the face. Histopathological examination of...
Saved in:
Published in | Rare tumors Vol. 7; no. 1; pp. 5675 - 13 |
---|---|
Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
PAGEPress Publications
18.02.2015
PAGEPress Publications, Pavia, Italy SAGE Publishing |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Cherubism is rare disease and has been rarely reported in African pediatric population. We report here the case of a 10-year-old child who was referred to our hospital for bilateral jaws swelling. Physical examination revealed bilateral swelling symmetry of the face. Histopathological examination of the biopsy specimen showed loose fibrous stroma, proliferating fibrous connective with tissue interspersed with multinucleated giant cells, small thin walled blood vessels and scattered sparse mononuclear inflammatory infiltrate. Our patient presented cherubism. Cherubism is rarely described in children living in sub-Saharan Africa. Genetic and molecular investigations plays an important role in diagnosis but were not available in poor resources settings in developing countries such as the Democratic Republic of Congo. |
---|---|
Bibliography: | Conflict of interests: the authors declare no potential conflict of interests. Contributions: MNA, RSK and JLGE are responsible for the design and writing of the study; AM has collaborated in the radiological interpretation; RSK specialist pathology has been responsible of the analysis of the specimens for the diagnosis; JND has been responsible for oral description; MNA and JLGE are the group leader and are responsible for the idea of the study. |
ISSN: | 2036-3605 2036-3613 2036-3613 |
DOI: | 10.4081/rt.2015.5675 |