Ectopic Adrenocorticotropic Hormone (ACTH)-Dependent Cushing Syndrome Secondary to Olfactory Neuroblastoma: A Rare Entity

Timely diagnosis and definitive surgical resection of ACTH-producing ONB, along with endocrine stabilization and adjuvant radiotherapy, can lead to endocrine remission and improved long-term outcomes.

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Publication Details

Journal
AACE Endocrinology and Diabetes
Published
2025-08-22
DOI
https://doi.org/10.1016/j.aed.2025.08.004
Primary Topic
Pituitary Gland Disorders and Treatments
Type
article
Field-Weighted Citation Impact
0.00
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article

Ectopic Adrenocorticotropic Hormone (ACTH)-Dependent Cushing Syndrome Secondary to Olfactory Neuroblastoma: A Rare Entity

Naseem Eisa
AACE Endocrinology and Diabetes
Pituitary Gland Disorders and Treatments
article

Ectopic Adrenocorticotropic Hormone (ACTH)-Dependent Cushing Syndrome Secondary to Olfactory Neuroblastoma: A Rare Entity

Naseem Eisa
article en

Abstract

Timely diagnosis and definitive surgical resection of ACTH-producing ONB, along with endocrine stabilization and adjuvant radiotherapy, can lead to endocrine remission and improved long-term outcomes.

AACE Endocrinology and DiabetesVol. 12(4)
Community Partners (US)
Zero hunger
Openalex Percentile: Top 70%
Pituitary Gland Disorders and Treatments
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Ectopic Adrenocorticotropic Hormone (ACTH)-Dependent Cushing Syndrome Secondary to Olfactory Neuroblastoma: A Rare Entity — Naseem Eisa · AACE Endocrinology and Diabetes (2025) | TGRS Research Map | TGRS