Malignant infantile osteopetrosis

Malignant infantile osteopetrosis
Other names	Infantile autosomal recessive osteopetrosis, Infantile osteopetrosis
Child with osteopetrosis

Malignant infantile osteopetrosis is a rare osteosclerosing type of

The generalized increase in bone density has a special predilection to involve the medullary portion with relative sparing of the cortices.[1] Obliteration of bone marrow spaces and subsequent depression of the cellular function can result in serious hematologic complications. Optic atrophy and cranial nerve damage secondary to bony expansion can result in marked morbidity. The prognosis is extremely poor in untreated cases.^[2] Plain radiography provides the key information to the diagnosis. Clinical and radiologic correlations are also fundamental to the diagnostic process, with additional gene testing being confirmatory.

Presentation

Hematologic manifestations related to bone marrow suppression and subsequent pancytopenia are a major source of morbidity and mortality. Additionally, extramedullary hematopoiesis can result in liver and spleen dysfunction. Cranial nerve dysfunction and neurologic complications are usually associated with infantile osteopetrosis. Expansion of the skull bone leads to macrocephaly. Additionally, linear growth retardation that is not apparent at birth, delayed motor milestones and poor dentition can occur.^[2]

Diagnosis

Skeletal radiography

The generalized increase in bone density of the medullary portion predominates with relative sparing of the cortices. The axial and appendicular skeleton are uniformly involved. Malignant infantile osteopetrosis is known for exhibiting specific plain radiographic abnormalities:^[1]

• Loss of differentiation between the medullary and cortical portions of bone is a radiographic hallmark of infantile osteopetrosis
• Characteristic endobone or "bone-within-bone" appearance in the spine, or "sandwich vertebra" appearance, characterized by dense endplate sclerosis with sharp margins
• Characteristic endobone or "bone-within-bone" appearance in the pelvis and long bones of extremities where areas of osteosclerosis intermingle with areas of relatively hypodense bone.
• Failure of
  remodeling
  of the distal femoral and proximal humeral metaphyses giving the affected bones a funnel shaped appearance known as an Erlenmeyer flask deformity
• Alternating radiolucent femoral metaphyseal bands
• Pathologic fractures

Differential diagnosis

The differential diagnosis of malignant infantile osteopetrosis includes other genetic

• Neuropathic infantile osteopetrosis
• Infantile osteopetrosis with renal tubular acidosis
• Infantile osteopetrosis with immunodeficiency
• IO with leukocyte adhesion deficiency syndrome (LAD-III)
• Intermediate osteopetrosis
• Autosomal dominant osteopetrosis (Albers-Schonberg)
• Pyknodysostosis (osteopetrosis acro-osteolytica)
• Osteopoikilosis (Buschke–Ollendorff syndrome)
• Osteopathia striata with cranial sclerosis
• Mixed sclerosing bone dysplasia
• Progressive diaphyseal dysplasia (Camurati–Engelmann disease)
• SOST-related sclerosing bone dysplasias

Treatment

The only effective line of treatment for malignant infantile osteopetrosis is hematopoietic stem cell transplantation.^[2][4][5] It has been shown to provide long-term disease-free periods for a significant percentage of those treated.^[2] It can impact both hematologic and skeletal abnormalities;^[2][4] and has been used successfully to reverse the associated skeletal abnormalities.^[4][5]

Radiographs of at least one case with malignant infantile osteopetrosis have demonstrated bone remodeling and recanalization of medullar canals following hematopoietic stem cell transplantation. This favorable radiographic response could be expected within one year following the procedure^[4][5] – nevertheless, primary graft failure can prove fatal.^[2]

References

External links