Literature DB >> 26950774

Pituitary stalk lesions: systematic review and clinical guidance.

Sarah Catford1, Yi Yuen Wang2, Rosemary Wong3.   

Abstract

The spectrum of pituitary stalk (PS) pathology is vast, presenting a diagnostic challenge. Published large series of PS lesions demonstrate neoplastic conditions are most frequent, followed by inflammatory, infectious and congenital diseases. Inflammatory pathologies however, account for the majority of PS lesions in published small case series and case reports. Physicians must be familiar with the major differential diagnoses and necessary investigations. A comprehensive history and thorough clinical examination is critical. Although magnetic resonance imaging of the PS in disease is nonspecific, associated intracranial features may narrow the differential diagnosis. Initial investigations include basic pathology and computer tomography imaging of the neck, chest, abdomen and pelvis. Further investigations should be guided by the clinical context. PS biopsy should be considered when a diagnosis is regarded essential in centres where an experienced neurosurgeon is available. Treatment is dependent on the underlying disease process and may necessitate pituitary hormone replacement.
© 2016 John Wiley & Sons Ltd.

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Year:  2016        PMID: 26950774     DOI: 10.1111/cen.13058

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN: 0300-0664            Impact factor:   3.478


  12 in total

Review 1.  Primary hypophysitis and other autoimmune disorders of the sellar and suprasellar regions.

Authors:  Sriram Gubbi; Fady Hannah-Shmouni; Constantine A Stratakis; Christian A Koch
Journal:  Rev Endocr Metab Disord       Date:  2018-12       Impact factor: 6.514

2.  Sellar, suprasellar, and parasellar masses: Imaging features and neurosurgical approaches.

Authors:  Bryan Lubomirsky; Zachary B Jenner; Morgan B Jude; Kiarash Shahlaie; Reza Assadsangabi; Vladimir Ivanovic
Journal:  Neuroradiol J       Date:  2021-12-02

3.  Single center study of 53 consecutive patients with pituitary stalk lesions.

Authors:  Mirjana Doknic; Dragana Miljic; Sandra Pekic; Marko Stojanovic; Dragan Savic; Emilija Manojlovic-Gacic; Tatjana Milenkovic; Vera Zdravkovic; Maja Jesic; Dusan Damjanovic; Slobodan Lavrnic; Ivan Soldatovic; Aleksandar Djukic; Milan Petakov
Journal:  Pituitary       Date:  2018-12       Impact factor: 4.107

Review 4.  Imaging findings in hypophysitis: a review.

Authors:  Ferdinando Caranci; Giuseppe Leone; Andrea Ponsiglione; Massimo Muto; Fabio Tortora; Mario Muto; Sossio Cirillo; Luca Brunese; Alfonso Cerase
Journal:  Radiol Med       Date:  2019-12-20       Impact factor: 3.469

5.  Difficulties in cerebrospinal fluid βhCG interpretation in a patient with an infundibular lesion.

Authors:  Alicia R Jones; Alan McNeil; Christopher Yates; Bala Krishnamurthy; Peter S Hamblin
Journal:  Endocrinol Diabetes Metab Case Rep       Date:  2018-02-23

6.  Multiple endocrinological failures as a clinical presentation of a metastatic lung adenocarcinoma.

Authors:  Taieb Ach; Perrine Wojewoda; Flora Toullet; Roxane Ducloux; Véronique Avérous
Journal:  Endocrinol Diabetes Metab Case Rep       Date:  2020-04-29

7.  A Case of Burnt-Out Langerhans Cell Histiocytosis Presenting as Postpartum Hypopituitarism.

Authors:  Susmita Reddy Karri; Amy Hsieh; John Binder; Vasant Shenoy
Journal:  AACE Clin Case Rep       Date:  2020-12-28

8.  A UNIQUE CASE OF CENTRAL HYPOPITUITARISM AND CENTRAL DIABETES INSIPIDUS CAUSED BY DIFFUSE LARGE B-CELL LYMPHOMA.

Authors:  Jason A Stegink; Vishal Sehgal; Manige Konig
Journal:  AACE Clin Case Rep       Date:  2019-01-30

9.  Cryptorchidism is a Useful Clue for Idiopathic Hypogonadotropic Hypogonadism in Pituitary Stalk Thickening.

Authors:  Shamharini Nagaratnam; Subashini Rajoo; Mohamed Badrulnizam Long Bidin; Norzaini Rose Mohd Zain
Journal:  J ASEAN Fed Endocr Soc       Date:  2021-04-23

10.  Central diabetes insipidus caused by a pituitary stalk germinoma resembling infundibuloneurohypophysitis.

Authors:  Daniela Dias; Helena Vilar; João Passos; Valeriano Leite
Journal:  BMJ Case Rep       Date:  2020-09-09
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