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Rapidly recurrent recalcitrant Rathke Cleft Cyst: Case report and review of the literature.
Chalif, E J; El Shatanofy, M; Mozaffari, K; Goyal, S; Sherman, J H.
Afiliação
  • Chalif EJ; Department of Neurological Surgery, University of California, San Francisco, San Francisco, California; Department of Neurosurgery, The George Washington University, Washington, District of Columbia, United States.
  • El Shatanofy M; Department of Neurosurgery, The George Washington University, Washington, District of Columbia, United States.
  • Mozaffari K; Department of Neurosurgery, The George Washington University, Washington, District of Columbia, United States.
  • Goyal S; Department of Radiation Oncology, The George Washington University, Washington, District of Columbia, United States.
  • Sherman JH; Rockefeller Neuroscience Institute, Department of Neurosurgery, West Virginia University, Martinsburg, West Virginia. Electronic address: JSherman0620@gmail.com.
Neurochirurgie ; 68(5): 535-539, 2022 Oct.
Article em En | MEDLINE | ID: mdl-35260274
ABSTRACT

BACKGROUND:

Rathke Cleft Cysts (RCC) are cystic sellar or suprasellar nonneoplastic lesions that are thought to originate from remnants of the rathke pouch. Postoperatively, RCCs have a tendency to reaccumulate, after which preoperative symptoms may recur. However, there exists very little evidence on which treatments are most effective in these patients. CASE-DESCRIPTION In this report, we present a unique case of a symptomatic RCC that recurred four times after initial transsphenoidal surgery. Following each surgery, the patient had significant visual improvement with post-op imaging displaying decompression of the neural elements. However, RCC reaccumulated in strikingly rapid time intervals of 1.5 months, 0.5 months, 1.5 years, and 5 months after each respective prior surgery. Repeat interventions with transsphenoidal, pterional and supraorbital approaches were unsuccessful in providing a durable treatment response. The patient ultimately underwent radiotherapy after a final surgical marsupialization of the cyst and has since displayed stable imaging with improved vision. This patient represented a 'perfect storm' of factors that may contribute to cyst recurrence, including substantial visual field deficits, large cyst size, peripheral wall enhancements on MRI, an intraoperative CSF leak, use of a fat graft, subtotal resection of the portion of cyst wall that adhered to important suprasellar structures, squamous metaplasia noted in cyst wall, and suprasellar extension.

CONCLUSIONS:

We demonstrate that different surgical approaches through repeat surgeries may not assist in prevention of further recurrence; instead, we propose that radiotherapy should be offered early in the treatment course of recurrent cases that have additional risk factors for further reoccurrence.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Cistos do Sistema Nervoso Central / Cistos / Neoplasias Renais Tipo de estudo: Diagnostic_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Neurochirurgie Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Cistos do Sistema Nervoso Central / Cistos / Neoplasias Renais Tipo de estudo: Diagnostic_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Neurochirurgie Ano de publicação: 2022 Tipo de documento: Article