Literature DB >> 36074243

Pre- and peri-operative characteristics, complications and outcomes of patients with biochemically silent pheochromocytomas; a case series.

Athanasios Fountas1, Georgia Kanti1, Spyridoula Glycofridi1, Maria A Christou2, Athanasia Kalantzi1, Irene Giagourta1, Athina Markou1, Georgia Ntali3,4, Chrysanthi Aggeli5, Eleftheria Saoulidou6, Antonia Dimakopoulou6, George N Zografos5, Theodora Kounadi1, Stelios Tigas2, Labrini Papanastasiou7.   

Abstract

PURPOSE: Pheochromocytomas are rare tumors and biochemically silent ones with normal catecholamine levels are even rarer. Up to date, biochemically inactive pheochromocytomas are poorly investigated. We aimed to systematically assess the pre- and peri-operative characteristics and the outcomes of patients with these tumors who had been treated and followed-up in 2 tertiary centers.
METHODS: Clinical, laboratory and imaging data, treatment outcomes and follow-up of biochemically silent pheochromocytoma patients were recorded.
RESULTS: Ten patients (5 men) [median age at diagnosis 52.5 years (24-72)] were included. Adrenal masses were incidentally discovered in all patients except from one who presented with pheochromocytoma-related manifestations. Twenty-four-hour urine metanephrine and normetanephrine levels were in the low-normal, normal and high-normal range in 4, 4 and 2 patients and in 1, 6 and 3 patients, respectively. Tumors were unilateral [median size 46 mm (17-125)] and high density on pre-contrast CT imaging or high signal intensity on T2-weighted MRI scans were found in all cases. Pre-operatively, 5 patients were treated with phenoxybenzamine [median total daily dose 70 mg (20-100)]. Intra-operatively, 4 patients developed hypertension requiring vasodilator administration and 8 developed hypotension; vasoconstrictors were required in 5 cases. One patient, not pre-operatively treated with phenoxybenzamine, developed Takotsubo cardiomyopathy. During a median 24-month (12-88) follow-up period, one patient had disease progression.
CONCLUSIONS: The majority (90%) of patients with biochemically silent pheochromocytomas developed hemodynamic instability during adrenal surgery. In patients with biochemically silent adrenal lesions and a high suspicion index for pheochromocytoma based on tumor imaging characteristics, pre-operative alpha-blockade treatment may be advisable.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Adrenals; Hemodynamic instability; Metanephrines; Normetanephrines; Pheochromocytomas; Silent

Year:  2022        PMID: 36074243     DOI: 10.1007/s12020-022-03182-w

Source DB:  PubMed          Journal:  Endocrine        ISSN: 1355-008X            Impact factor:   3.925


  16 in total

1.  Diagnosis of silent pheochromocytoma and paraganglioma.

Authors:  Roderick Clifton-Bligh
Journal:  Expert Rev Endocrinol Metab       Date:  2013-01

Review 2.  Incidence of pheochromocytoma and sympathetic paraganglioma in the Netherlands: A nationwide study and systematic review.

Authors:  Annika M A Berends; Edward Buitenwerf; Ronald R de Krijger; Nic J G M Veeger; Anouk N A van der Horst-Schrivers; Thera P Links; Michiel N Kerstens
Journal:  Eur J Intern Med       Date:  2018-02-01       Impact factor: 4.487

3.  Silent adrenal nodules in von Hippel-Lindau disease suggest pheochromocytoma.

Authors:  B S Aprill; A J Drake; D H Lasseter; K M Shakir
Journal:  Ann Intern Med       Date:  1994-03-15       Impact factor: 25.391

4.  Pheochromocytoma Characteristics and Behavior Differ Depending on Method of Discovery.

Authors:  Lucinda M Gruber; Robert P Hartman; Geoffrey B Thompson; Travis J McKenzie; Melanie L Lyden; Benzon M Dy; William F Young; Irina Bancos
Journal:  J Clin Endocrinol Metab       Date:  2019-05-01       Impact factor: 5.958

5.  Pheochromocytoma: an uncommon presentation of an asymptomatic and biochemically silent adrenal incidentaloma.

Authors:  Sunil Kumar Kota; Siva Krishna Kota; Sandip Panda; Kirtikumar D Modi
Journal:  Malays J Med Sci       Date:  2012-04

6.  Epidemiology of pheochromocytoma and paraganglioma: population-based cohort study.

Authors:  Alexander A Leung; Janice L Pasieka; Martin D Hyrcza; Danièle Pacaud; Yuan Dong; Jessica M Boyd; Hossein Sadrzadeh; Gregory A Kline
Journal:  Eur J Endocrinol       Date:  2021-01       Impact factor: 6.664

Review 7.  A rare case of clinically and biochemically silent giant right pheochromocytoma: case report and review of literature.

Authors:  Nora Sundahl; Sam Van Slycke; Nele Brusselaers
Journal:  Acta Chir Belg       Date:  2016-04-21       Impact factor: 1.090

8.  Bilateral biochemically silent pheochromocytoma, not silent after all.

Authors:  Robert Zakhia El-Doueihi; Ibrahim Salti; Marie Maroun-Aouad; Albert El Hajj
Journal:  Urol Case Rep       Date:  2019-03-22

9.  Silent Adrenal Pheochromocytoma Coexistent with Corticomedullary Hyperplasia: A Case Incidentally Discovered.

Authors:  Luigi Petramala; Antonio Concistrè; Federica Olmati; Vincenza Saraceno; Gino Iannucci; Antonio Ciardi; Giorgio De Toma; Claudio Letizia
Journal:  Eur J Case Rep Intern Med       Date:  2017-10-06
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