Cervix neuroendocrine carcinoma presenting with severe hypokalemia and Cushing’s syndrome

Neuroendocrine carcinomas of the cervix are very rare, accounting for only 1–2% of all cervical cancers and

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Bibliographic Details
Published in:Endocrine 2020-02, Vol.67 (2), p.318-320
Main Authors: Di Filippo, Luigi, Vitali, Giordano, Taccagni, Gianluca, Pedica, Federica, Guaschino, Giulia, Bosi, Emanuele, Martinenghi, Sabina
Format: Article
Language:English
Subjects:
Adrenocorticotropic hormone
Cervical cancer
Cervical carcinoma
Cervix
Clinical Management of Endocrine Diseases
Cushing syndrome
Diabetes
Endocrinology
Human papillomavirus
Humanities and Social Sciences
Hypokalemia
Internal Medicine
Medicine
Medicine & Public Health
Metastases
Metastasis
multidisciplinary
Nervous system diseases
Neuroendocrine tumors
Pituitary
Science
Uterus
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Description
Summary:Neuroendocrine carcinomas of the cervix are very rare, accounting for only 1–2% of all cervical cancers and
ISSN:1355-008X
1559-0100
DOI:10.1007/s12020-020-02202-x