Sellar surprises: a single-centre experience of unusual sellar masses

Author:

Thakkar Kunal1,Ramteke-Jadhav Swati1,Kasaliwal Rajeev2,Memon Saba Samad1,Patil Virendra1,Thadani Puja1,Lomte Nilesh1,Sankhe Shilpa3,Goel Atul4,Epari Sridhar5,Goel Naina6,Lila Anurag1,Shah Nalini S1,Bandgar Tushar1

Affiliation:

1. 1Department of Endocrinology, Seth G S Medical College & KEM Hospital, Mumbai, India

2. 2Department of Endocrinology, Mahatma Gandhi Medical College & Hospital, Jaipur, India

3. 3Department of Radiology, Seth G S Medical College & KEM Hospital, Mumbai, India

4. 4Department of Neurosurgery, Seth G S Medical College & KEM Hospital, Mumbai, India

5. 5Department of Pathology, Tata Memorial Centre, Mumbai, India

6. 6Department of Neuropathology, Seth G S Medical College & KEM Hospital, Mumbai, India

Abstract

Background Most common incidentally detected sellar-suprasellar region (SSR) masses are pituitary adenomas, followed by craniopharyngioma, rathke’s cleft cyst, hypophysitis, and meningioma. Besides these, certain unusual SSR lesions can sometimes present as diagnostic challenges, where diagnosis is often made post-operatively on histopathology, the pre-operative suspicion of which might have influenced the management strategies. Series describing such masses are few. Objective To present clinical, biochemical, and radiological characteristics and management outcomes of rare SSR lesions other than pituitary adenomas, craniopharyngioma, rathke’s cleft cyst, hypophysitis, and meningioma. Design, setting, patients Retrospective case record analysis of patients with uncommon SSR masses (from January 2006 to December 2016). Results Our series consisted of ten patients, five with neoplastic and five with non-neoplastic lesions. Neoplastic masses included granular cell tumor (n = 2), astrocytoma (n = 1), malignant peripheral nerve sheath tumor (MPNST, n = 1), and metastasis from occult papillary carcinoma of thyroid (n = 1), while non-neoplastic masses were aspergillus abscess (n = 1), sterile abscess (n = 1), and tubercular abscess (n = 1), aneurysm of left internal carotid artery (n = 1), and ruptured dermoid cyst (n = 1). All patients (except one) presented with headache and/or visual disturbance. Only one patient had acromegaly while most others had hypopituitarism. We describe detailed MRI characteristics of each of the lesion. Seven patients underwent trans-sphenoidal surgery. Post-operatively, five patients had permanent diabetes insipidus, while two patients died in early post-operative period. Conclusion Our series expand the differential diagnostic considerations of SSR lesions. Most of the rare SSR masses present with symptoms of mass effects and hypopituitarism. Except for some non-neoplastic lesions like sellar abscesses, aneurysms, and dermoid cysts which can have some specific imaging characteristics that can provide clue to pre-operative diagnosis, most of the other neoplastic masses have overlapping radiological features, and pre-operative suspicion remains difficult.

Publisher

Bioscientifica

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

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