Fibrous Dysplasia of Skull: An Uncommon Presentation

Fibrous dysplasia is a developmental disorder of bone that can occur in monostotic or polyostotic form. Monostotic form is more frequent, usually seen in older children and young adults, commonly occurring in ribs, femur, tibia and craniofacial bones. Polyostotic fibrous dysplasia is less common, affecting as few as two bones to as much as 75% of the skeleton, predominantly involving the femur, pelvis and foot. We present a case of fibrous dysplasia involving the skull in a 29-year-old woman. On magnetic resonance imaging (MRI), a well-defined lytic lesion was identified in the outer cortex of the left parietal lobe for which two differential diagnoses were made: Langerhans cell histiocytosis (LCH) and lymphoma. The patient underwent craniotomy followed by mesh cranioplasty. The atypical location of the lesion initially obscured the diagnosis, which was ultimately confirmed through histopathological analysis.

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Publication Details

Journal
Annals of Pathology and Laboratory Medicine
Published
2025-08-20
DOI
https://doi.org/10.21276/apalm.3553
Primary Topic
Bone Tumor Diagnosis and Treatments
Type
article
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article

Fibrous Dysplasia of Skull: An Uncommon Presentation

Annals of Pathology and Laboratory Medicine
Bone Tumor Diagnosis and Treatments
article

Fibrous Dysplasia of Skull: An Uncommon Presentation

article en

Abstract

Fibrous dysplasia is a developmental disorder of bone that can occur in monostotic or polyostotic form. Monostotic form is more frequent, usually seen in older children and young adults, commonly occurring in ribs, femur, tibia and craniofacial bones. Polyostotic fibrous dysplasia is less common, affecting as few as two bones to as much as 75% of the skeleton, predominantly involving the femur, pelvis and foot. We present a case of fibrous dysplasia involving the skull in a 29-year-old woman. On magnetic resonance imaging (MRI), a well-defined lytic lesion was identified in the outer cortex of the left parietal lobe for which two differential diagnoses were made: Langerhans cell histiocytosis (LCH) and lymphoma. The patient underwent craniotomy followed by mesh cranioplasty. The atypical location of the lesion initially obscured the diagnosis, which was ultimately confirmed through histopathological analysis.

Annals of Pathology and Laboratory MedicineVol. 12(8)
Jawaharlal Nehru Medical College Hospital (IN), Aligarh Muslim University (IN)
Good health and well-being
Openalex Percentile: Top 31%
Bone Tumor Diagnosis and Treatments
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