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Surgical resection of granular cell tumor of the sellar region: three indications

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Abstract

Purpose

This case series evaluates the surgical management of granular cell tumor (GCT) of the sellar region. This rare entity presents a unique diagnostic and surgical challenge.

Methods

Institutional neuropathology databases at Brigham and Women’s Hospital and Massachusetts General Hospital were searched for cases with a tissue diagnosis of GCT, and with a location in the sellar region. Patient, treatment, tumor, and follow-up data were extracted.

Results

Three patients had a diagnosis of GCT of the sellar region occurring over an 18-year period. All three patients were followed postoperatively at our multidisciplinary pituitary center (median follow-up = 30 months; range 12–30 months). Hormonal disturbances, an incidental lesion requiring diagnosis, and neurological symptoms were indications for surgery in these patients. Two patients underwent a craniotomy and one underwent endoscopic transsphenoidal surgery. All three patients were free of tumor recurrence at last follow-up. In one case tested, positive thyroid transcription factor-1 (TTF-1) immunohistochemistry was observed.

Conclusion

GCT is generally a benign tumor of the sellar region. Surgical resection is the standard treatment, more recently with transsphenoidal surgery when indicated. Surgical resection results in optimal outcome for patients.

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Funding

NIH Training Grant T32 CA009001 (DJC).

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Correspondence to Abdul-Kareem Ahmed.

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The authors declare that they have no conflict of interest.

Research involving human participants and/or animals

IRB approval was obtained from Brigham & Women’s Hospital (Partners) for the search and use of institutional database data. (IRB Approval #: 2015P002352).

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Ahmed, AK., Dawood, H.Y., Cote, D.J. et al. Surgical resection of granular cell tumor of the sellar region: three indications. Pituitary 22, 633–639 (2019). https://doi.org/10.1007/s11102-019-00999-z

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  • DOI: https://doi.org/10.1007/s11102-019-00999-z

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