Literature DB >> 29777270

[Rathke cysts, craniopharyngioma, and colloid cysts : What are the differences between these pathologies?]

R Eymann1, M Kiefer2.   

Abstract

CLINICAL ISSUE: Headache is the most common symptom of colloid cysts, Rathke cysts, and craniopharyngioma due to their location in the midline, being extra-axial and typically presenting in the parasellar region. THERAPEUTIC PROBLEMS: Although these tumors are generally considered benign, each has its typical characteristics defined by its location and histology. These individual characteristics define whether surgery is necessary at all and if so, the preferred surgical approach and resection's totality. The histopathological findings primarily indicate that embryonic malformations-at the first glance, ectodermal in nature-cause these tumors. ACHIEVEMENT: Due to the fact that these disturbances occur at the boundary between ectodermal stomodeum and endodermal cephalogaster, however, does leave some doubts.

Entities:  

Keywords:  Brain; Embryology; Headaches; Histology; Tumors

Mesh:

Year:  2018        PMID: 29777270     DOI: 10.1007/s00117-018-0398-0

Source DB:  PubMed          Journal:  Radiologe        ISSN: 0033-832X            Impact factor:   0.635


  30 in total

Review 1.  Rathke's cleft cysts.

Authors:  Raluca Trifanescu; Olaf Ansorge; John A H Wass; Ashley B Grossman; Niki Karavitaki
Journal:  Clin Endocrinol (Oxf)       Date:  2012-02       Impact factor: 3.478

2.  Colloid Cyst of the Third Ventricle: Long-Term Results of Endoscopic Management in a Series of 112 Cases.

Authors:  Mohammad Samadian; Kaveh Ebrahimzadeh; Ehsan Nazari Maloumeh; Armin Jafari; Guive Sharifi; Sepideh Shiravand; Hadi Digaleh; Omidvar Rezaei
Journal:  World Neurosurg       Date:  2017-12-23       Impact factor: 2.104

Review 3.  Craniopharyngioma.

Authors:  John A Jane; Edward R Laws
Journal:  Pituitary       Date:  2006       Impact factor: 4.107

4.  Rathke cleft cyst in seven-year-old girl presenting with central diabetes insipidus and review of literature.

Authors:  Olcay Evliyaoglu; Cetin Evliyaoglu; Sebnem Ayva
Journal:  J Pediatr Endocrinol Metab       Date:  2010-05       Impact factor: 1.634

5.  Surgery for Rathke cleft cysts: technical considerations and outcomes.

Authors:  Ronald J Benveniste; Wesley A King; Jane Walsh; Jacob S Lee; Thomas P Naidich; Kalmon D Post
Journal:  J Neurosurg       Date:  2004-10       Impact factor: 5.115

6.  Pituitary adenoma, craniopharyngioma, and Rathke cleft cyst involving both intrasellar and suprasellar regions: differentiation using MRI.

Authors:  S H Choi; B J Kwon; D G Na; J-H Kim; M H Han; K-H Chang
Journal:  Clin Radiol       Date:  2007-02-26       Impact factor: 2.350

7.  Comparative immunohistochemical assessment of craniopharyngioma and related lesions.

Authors:  Brian H Le; Javad Towfighi; Silloo B Kapadia; M Beatriz S Lopes
Journal:  Endocr Pathol       Date:  2007       Impact factor: 3.943

8.  Surgical treatment of rathke cleft cysts in children.

Authors:  Gabriel Zada; Benjamin Ditty; Sean A McNatt; J Gordon McComb; Mark D Krieger
Journal:  Neurosurgery       Date:  2009-06       Impact factor: 4.654

9.  Immunohistochemical study of intracranial cysts.

Authors:  T Inoue; T Matsushima; M Fukui; T Iwaki; I Takeshita; C Kuromatsu
Journal:  Neurosurgery       Date:  1988-11       Impact factor: 4.654

10.  Craniopharyngeal canal and its spectrum of pathology.

Authors:  T A Abele; K L Salzman; H R Harnsberger; C M Glastonbury
Journal:  AJNR Am J Neuroradiol       Date:  2013-11-01       Impact factor: 3.825

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