Chronic recurrent multifocal osteomyelitis: a case report

Abstract Background Chronic recurrent multifocal osteomyelitis (CRMO), also known as chronic nonbacterial osteomyelitis, is a rare, noninfectious inflammatory disorder that causes multifocal bone lesions with swelling and pain. Lytic and sclerotic bone lesions could be found on X-ray. Short tau inve...

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Main Authors: Maria Francesca Gicchino, Mario Diplomatico, Carmela Granato, Daniela Capalbo, Pierluigi Marzuillo, Alma Nunzia Olivieri, Emanuele Miraglia del Giudice
Format: Article
Language:English
Published: BMC 2018-02-01
Series:Italian Journal of Pediatrics
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13052-018-0463-3
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author Maria Francesca Gicchino
Mario Diplomatico
Carmela Granato
Daniela Capalbo
Pierluigi Marzuillo
Alma Nunzia Olivieri
Emanuele Miraglia del Giudice
author_facet Maria Francesca Gicchino
Mario Diplomatico
Carmela Granato
Daniela Capalbo
Pierluigi Marzuillo
Alma Nunzia Olivieri
Emanuele Miraglia del Giudice
author_sort Maria Francesca Gicchino
collection DOAJ
description Abstract Background Chronic recurrent multifocal osteomyelitis (CRMO), also known as chronic nonbacterial osteomyelitis, is a rare, noninfectious inflammatory disorder that causes multifocal bone lesions with swelling and pain. Lytic and sclerotic bone lesions could be found on X-ray. Short tau inversion recovery magnetic resonance imaging (STIR MRI) shows bone marrow oedema, bone expansion, lytic areas and periosteal reaction. CRMO is characterized by periodic exacerbations and remissions of unclear/unknown pathogenesis. Case presentation A 10 years old girl, suffering from pain in her right shoulder since the age of 9 years presented to our Department. Thanks to clinical data, laboratoristic and radiological findings and bone biopsy CRMO was diagnosed. So patient started anti-inflammatory treatment and her conditions improved. Conclusions In a child with bone pain should be considered also rare condition as CRMO to perform a correct diagnosis and start an adequate treatment avoiding complications such as bone damage. This condition should be suspected in a child with recurrent bone pain, modest increase of inflammatory indices, lytic or sclerotic bone lesion on X Ray. Typical CRMO localizations are metaphyses of long bones, pelvis, clavicle, vertebral column, sternum, ribs, jaw, but any bone can be involved. The most common CRMO differential diagnosis is represented by infections, malignant bone tumors, Langerhans Cells Histiocytosis (LCH).
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spelling doaj.art-cb307fd18d8b486299198dda7cf158902022-12-21T17:56:30ZengBMCItalian Journal of Pediatrics1824-72882018-02-014411510.1186/s13052-018-0463-3Chronic recurrent multifocal osteomyelitis: a case reportMaria Francesca Gicchino0Mario Diplomatico1Carmela Granato2Daniela Capalbo3Pierluigi Marzuillo4Alma Nunzia Olivieri5Emanuele Miraglia del Giudice6Department of Woman and Child and General and Specialized Surgery, University of the Study of Campania “Luigi Vanvitelli”Department of Woman and Child and General and Specialized Surgery, University of the Study of Campania “Luigi Vanvitelli”Department of Woman and Child and General and Specialized Surgery, University of the Study of Campania “Luigi Vanvitelli”Department of Woman and Child and General and Specialized Surgery, University of the Study of Campania “Luigi Vanvitelli”Department of Woman and Child and General and Specialized Surgery, University of the Study of Campania “Luigi Vanvitelli”Department of Woman and Child and General and Specialized Surgery, University of the Study of Campania “Luigi Vanvitelli”Department of Woman and Child and General and Specialized Surgery, University of the Study of Campania “Luigi Vanvitelli”Abstract Background Chronic recurrent multifocal osteomyelitis (CRMO), also known as chronic nonbacterial osteomyelitis, is a rare, noninfectious inflammatory disorder that causes multifocal bone lesions with swelling and pain. Lytic and sclerotic bone lesions could be found on X-ray. Short tau inversion recovery magnetic resonance imaging (STIR MRI) shows bone marrow oedema, bone expansion, lytic areas and periosteal reaction. CRMO is characterized by periodic exacerbations and remissions of unclear/unknown pathogenesis. Case presentation A 10 years old girl, suffering from pain in her right shoulder since the age of 9 years presented to our Department. Thanks to clinical data, laboratoristic and radiological findings and bone biopsy CRMO was diagnosed. So patient started anti-inflammatory treatment and her conditions improved. Conclusions In a child with bone pain should be considered also rare condition as CRMO to perform a correct diagnosis and start an adequate treatment avoiding complications such as bone damage. This condition should be suspected in a child with recurrent bone pain, modest increase of inflammatory indices, lytic or sclerotic bone lesion on X Ray. Typical CRMO localizations are metaphyses of long bones, pelvis, clavicle, vertebral column, sternum, ribs, jaw, but any bone can be involved. The most common CRMO differential diagnosis is represented by infections, malignant bone tumors, Langerhans Cells Histiocytosis (LCH).http://link.springer.com/article/10.1186/s13052-018-0463-3Chronic recurrent multifocal osteomyelitisCRMOBone pain
spellingShingle Maria Francesca Gicchino
Mario Diplomatico
Carmela Granato
Daniela Capalbo
Pierluigi Marzuillo
Alma Nunzia Olivieri
Emanuele Miraglia del Giudice
Chronic recurrent multifocal osteomyelitis: a case report
Italian Journal of Pediatrics
Chronic recurrent multifocal osteomyelitis
CRMO
Bone pain
title Chronic recurrent multifocal osteomyelitis: a case report
title_full Chronic recurrent multifocal osteomyelitis: a case report
title_fullStr Chronic recurrent multifocal osteomyelitis: a case report
title_full_unstemmed Chronic recurrent multifocal osteomyelitis: a case report
title_short Chronic recurrent multifocal osteomyelitis: a case report
title_sort chronic recurrent multifocal osteomyelitis a case report
topic Chronic recurrent multifocal osteomyelitis
CRMO
Bone pain
url http://link.springer.com/article/10.1186/s13052-018-0463-3
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