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Article
May 1980

Temporal Bone Histopathologic Features in Fanconi's Anemia Syndrome

Author Affiliations

From the Departments of Otolaryngology (Drs Harada, Sando, Stool, and Myers) and Pathology (Dr Sando), University of Pittsburgh School of Medicine and the Eye and Ear Hospital of Pittsburgh.

Arch Otolaryngol. 1980;106(5):275-279. doi:10.1001/archotol.1980.00790290027010
Abstract

• A histopathologic study of the temporal bones from a 7-year-old girl with Fanconi's anemia syndrome demonstrated (1) hemorrhage in the submucosal layer and the cavity of the middle ear and mastoid, massive in the right ear; (2) hypocellularity of the bone marrow; (3) minor but multiple anomalies of the middle ear; and (4) hypodevelopment of the hook portion of the cochlea and reduced overall length of the cochlear duct. The histopathologic features of these temporal bones appears to suggest that congenital anomalies of the inner ear, as well as those of the external and middle ears, would be possible causes of the deafness that accompanies Fanconi's anemia syndrome.

(Arch Otolaryngol 106:275-279, 1980)

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