A Rare Case of Recurrent Pituitary Collision Tumors

Author:

Shakally Almoutaz1,Tahara Naoyuki23,Clark Brent4,Tummala Ramachandra5ORCID,Caicedo-Granados Emiro6,Kawakami Yasuhiko23ORCID,Araki Takako1ORCID

Affiliation:

1. Division of Diabetes, Endocrinology and Metabolism, Department of Medicine, University of Minnesota, Minneapolis, Minnesota

2. Department of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, Minnesota

3. Stem Cell Institute, University of Minnesota, Minneapolis, Minnesota

4. Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota

5. Department of Neurosurgery, University of Minnesota, Minneapolis, Minnesota

6. Department of Otolaryngology, Head and Neck Surgery, University of Minnesota, Minneapolis, Minnesota

Abstract

Abstract Pituitary collision tumors are sporadically reported and rare. We present a case of pituitary collision tumors with nonfunctioning pituitary adenoma (NFPA) and craniopharyngioma. In order to look for any common activated pathway, we examined WNT/β-CATENIN signaling activation, known to be involved in tumorigenesis in both craniopharyngioma and NFPA. We found nuclear accumulation of β-CATENIN protein and expression of LEF1 protein, markers of active β-CATENIN signaling in the craniopharyngioma but not in the pituitary adenomas. In our case, the NFPA is invasive macroadenoma, which is a frequently identified type of pituitary adenoma in collision tumor cases. Recurrence of this tumor was first observed after 8 years of follow-up. Based on this case, we suggest that pituitary collision tumors require long-term follow-up.

Funder

Graduate School, University of Minnesota

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Publisher

The Endocrine Society

Subject

Endocrinology, Diabetes and Metabolism

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