Multiple endocrine neoplasia type 1 (MEN1) presenting with renal stones: Case report and review
Multiple endocrine neoplasia type 1 (MEN1) is a complex, autosomal dominant inherited syndrome characterized by 3 different tumors (parathyroid, anterior pituitary, and pancreatic islet). The diagnosis is defined clinically by the presence of 2 or more primary tumors. We report the case of a 35 year...
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Veröffentlicht in: | Radiology case reports 2020-12, Vol.15 (12), p.2503-2509 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Multiple endocrine neoplasia type 1 (MEN1) is a complex, autosomal dominant inherited syndrome characterized by 3 different tumors (parathyroid, anterior pituitary, and pancreatic islet). The diagnosis is defined clinically by the presence of 2 or more primary tumors. We report the case of a 35 years old patient who presented with recurrent renal stones and imaging findings for MEN1. Computed tomography pancreas revealed a mass in the tail which was confirmed by magnetic resonance imaging. Ultrasound of her neck showed a mass on the left side and MIBI scan diagnosed a parathyroid adenoma which was later pathologically confirmed. |
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ISSN: | 1930-0433 1930-0433 |
DOI: | 10.1016/j.radcr.2020.09.037 |