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Cushing's Syndrome Secondary to Olfactory Neuroblastoma
Authors:Mark A. Arnesen   Bernd W. Scheithauer  Susan Freeman
Affiliation: a Department of Pathology, Abbott Northwestern Hospital, Minneapolis, Minnesota, USAb Department of Pathology and Laboratory Medicine, Mayo Clinic, Rochester, Minnesota, USAc Abbott Northwestern Hospital, Minneapolis, Minnesota, USA
Abstract:A case of olfactory neuroblastoma in a 36-year-old woman who presented with florid Cushing's syndrome is reported. A nasal polyp, which proved to be an olfactory neuroblastoma, was resected. The procedure was followed by complete remission from the endocrinologic abnormalities. Postoperatively, the patient was well for 5 years until recurrence of both Cushing's syndrome and the nasal polyp was noted. Following combined transnasal-transcranial resection of the tumor, which extended into the anterior cranial fossa, the patient again experienced complete remission of Cushing's syndrome. Immunohistochemistry showed the tumor to be positive for neuron-specific enolase, synaptophysin, chromogran-in, adrenocorticotropic hormone, (J-endorphin, and S-100 protein. Electron microscopy revealed neuritic processes containing microtubules and neurosecretory granules. This is the first reported case of Cushing's syndrome secondary to olfactory neuroblastoma.
Keywords:Cushing's syndrome  electron microscopy  immunohistochemistry  neuroendocrine carcinoma  primitive neuroectodermal tumor  olfactory neuroblastoma
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