OSTEOPETRORICKETS IN AN INFANT WITH COEXISTENT
CONGENITAL CYTOMEGALOVIRUS INFECTION
Katsafiloudi M, Gombakis N, Hatzipantelis E, Tragiannidis A
*Corresponding Author: Athanasios Tragiannidis, M.D., Ph.D., Assistant Professor of Pediatrics, Pediatric
Hematology-Oncology Unit, 2nd Pediatric Department, AHEPA Hospital, Aristotle University of
Thessaloniki, S. Kiriakidi 1 str., Thessaloniki, Greece. Tel: +306-944-944-777. Fax: +302-310-994-803.
E-mail: atragian@ auth.gr; atragian@hotmail.com
page: 107
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CONCLUSIONS
Malignant infantile osteopetrosis is a rare hereditary
skeletal disease, in some cases complicated by rickets. As high clinical suspicion is required for diagnosis, MIOP
should be kept in mind as a rare cause of pancytopenia and
hepatosplenomegaly. Some cases of successful bone marrow
transplantation in patients with infantile osteopetrosis
exist in the literature, and a similar case of MIOP with
coexistent CMV infection has been reported by Lee et al.
[8] but in their patient no BMT was performed. To the best
of our knowledge, this is the first case of infantile osteopetrosis
complicated by rickets in an infant with congenital
CMV infection that was successfully treated by HSCT.
Declaration of Interest. The authors report no conflicts
of interest. The authors alone are responsible for the
content and writing of this article.
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