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Rathke's cleft cyst infections and pituitary abscesses: case series and review of the literature.
Aranda, F; García, R; Guarda, F J; Nilo, F; Cruz, J P; Callejas, C; Balcells, M E; González, G; Rojas, R; Villanueva, P.
Afiliação
  • Aranda F; Neurosurgery Department, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • García R; Endocrinology Department, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Guarda FJ; Endocrinology Department, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Nilo F; Pituitary Tumor Program, Red de Salud UC-CHRISTUS, Santiago, Chile.
  • Cruz JP; Center for Translational Endocrinology (CETREN), School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Callejas C; Endocrinology Department, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Balcells ME; Pituitary Tumor Program, Red de Salud UC-CHRISTUS, Santiago, Chile.
  • González G; Center for Translational Endocrinology (CETREN), School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Rojas R; Pituitary Tumor Program, Red de Salud UC-CHRISTUS, Santiago, Chile.
  • Villanueva P; Radiology Department, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
Pituitary ; 24(3): 374-383, 2021 Jun.
Article em En | MEDLINE | ID: mdl-33433887
ABSTRACT

PURPOSE:

Pituitary abscesses (PAs) are a rare clinical entity which may arise from normal pituitary tissue or underlying lesions within the gland. Rathke's cleft cysts (RCCs) are not commonly associated with the development of PA.

METHODS:

Retrospective chart review of three patients with PAs within RCCs at a single university center and review of the literature.

RESULTS:

Three cases are reported. The first case presented with fever and headache and a history of prior surgery due to RCC and a recent respiratory tract infection. The second case had a history of recent skin infections and presented with sudden onset headache and hypopituitarism. In the third case, chronic visual field impairment prompted an ophthalmologic evaluation resulting in a diagnosis of an adenoma and an infected RCC. In all three cases, an endoscopic endonasal approach was performed to drain infected tissue and allowed microbiological identification of gram-positive cocci, followed by treatment with antibiotics for at least three weeks. Cases in the literature are scarce and the diagnosis is usually made intraoperatively due to non-specific manifestations and imaging. PAs arising from underlying pituitary lesions are less common than primary PAs. Differential diagnosis should include pituitary apoplexy, hypophysitis and other cystic lesions.

CONCLUSION:

PAs occurring in RCCs are infrequent. Clinical manifestations are commonly subacute, without septic symptoms. Imaging is usually non-specific. Preoperative diagnosis is infrequent and a broad differential diagnosis should be considered. Empirical antimicrobial therapy should be initiated and adjusted after obtaining cultures to reduce the rate of recurrence and improve clinical outcomes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças da Hipófise / Neoplasias Hipofisárias / Carcinoma de Células Renais / Cistos do Sistema Nervoso Central / Neoplasias Renais Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças da Hipófise / Neoplasias Hipofisárias / Carcinoma de Células Renais / Cistos do Sistema Nervoso Central / Neoplasias Renais Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article