alexa
Reach Us +44-7482-864460
Unusual and Challenging Presentation of Hereditary Pheochromocytoma: Physicians Should Not Be Fooled - A Case Report
ISSN: 1747-0862

Journal of Molecular and Genetic Medicine
Open Access

Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)
All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal.
  • Case Report   
  • J Mol Genet Med 2019, Vol 13(2): 428

Unusual and Challenging Presentation of Hereditary Pheochromocytoma: Physicians Should Not Be Fooled - A Case Report

Parasiliti-Caprino M1*, Matta M2, Lopez C1, Barbero U2, Maletta F3, Frea S2, Giraudo G4, Benso A1, Pasini B5, Ghigo E1 and Maccario M1
1Division of Endocrinology, Diabetology and Metabolism, Department of Medical Sciences, University of Turin, Turin, Italy
2Cardiology Unit, Department of Medical Sciences, University of Turin, Turin, Italy
3Pathology Unit, Department of Medical Sciences, University of Turin, Turin, Italy
4Division of Surgery, Department of Surgical Sciences, University of Turin, Turin, Italy
5Division of Medical Genetics, Department of Medical Sciences, University of Turin, Turin, Italy
*Corresponding Author: Dr. Parasiliti-Caprino M, Cardiology Unit, Department of Medical Sciences, University of Turin, Turin, Italy, Tel: 00390116335544, Email: [email protected]

Received Date: May 08, 2019 / Accepted Date: Jun 04, 2019 / Published Date: Jun 11, 2019

Abstract

We present the case of a 45-year-old woman admitted to our hospital with acute heart failure and cardiogenic shock requiring stabilization with an intra-aortic balloon pump, inotropes and vasopressors. Nevertheless, the patient developed a multi organ failure. Firstly, diagnosed as an acute myocarditis, bilateral pheochromocytoma was discovered with MRI scan and confirmed with urine and plasma metanephrines. Bilateral adrenalectomy was performed. The genetic testing revealed a mutation in the Neurofibromatosis type 1 gene. Given the life-threatening complications and the good prognosis after radical surgery, the diagnosis of pheochromocytoma should be quickly considered in patients presenting with unexplained cardiovascular compromise.

Keywords: Pheochromocytoma; Neurofibromatosis 1; Cardiovascular diseases; Neuroendocrine tumors; Hypertension

Introduction

Pheochromocytoma (PCC) and paraganglioma (PGL) are rare tumors arising from adrenomedullary cells and from sympathetic or parasympathetic ganglia respectively. About 80-85% of chromaffin cell tumors are PCCs, whereas 15-20% is PGLs. The prevalence of pheochromocytoma and paraganglioma (PPGL) in hypertensive patients varies between 0.2% and 0.6%, while PCC is observed in 5% of patients with adrenal incidentaloma. PCCs and sympathetic PGLs commonly produce catecholamines: epinephrine, norepinephrine and dopamine, while parasympathetic PGLs are often silent [1].

The rule that 10% of chromaffin tumors are paragangliomas, malignant, associated to genetic muta-tions, affect patients without arterial hypertension, have bilateral adrenals involvement and pediatric onset is not epidemiologically correct anymore. In fact, recent series reported that PPGL are as-sociated to genetic mutation in up to 40% of cases [2]. 14 different PPGL susceptibility genes have been reported: NF1, RET, VHL, SDHD, SDHC, SDHB, EGLN1/PHD2, KIF1, SDH5/ SDHAF2, IDH1, TMEM127, SDHA, MAX and HIF2. SDHB and MAX mutations are also considered good markers of aggressive clinical behavior. For these reasons, Endocrine Society and European Society of Endocrinology Guidelines recommend considering genetic tests in all patients with PPGL [1,3]. Many mutations in susceptibility genes for development of PPGLs have been identified in last years and research in this field has advanced our understanding in cancer biology.

PPGL were the first human tumor model found to carry an inherited mutation of a gene encoding a metabolic enzyme (SDHD). They are also pioneer models of genetic-based personalized medical care for example, in the management of multiple endocrine neoplasia type 2 (MEN2). In this pathology, the identification of a high-risk germline RET mutation can guide the need for early thyroidectomy to prevent medullary thyroid carcinoma, which is a co-occurring tumour in this disorder. PPGL also became the first tumors known to carry activating mutations of HIF2A, which had long been impli-cated in multiple human cancers and was suspected, but had never been genetically proved, to func-tion as a bona fide oncogene [4].

Case Report

A 45-year-old woman was admitted to our emergency care unit presenting with rapidly worsening dyspnoea, orthopnoea and fatigue. In anamnesis there is neither prior cardiologic disease nor chronic medical treatment. At first medical contact, she presented severe hypotension (systolic blood pressure 80 mmHg) and oliguria. ECG showed rapid atrial fibrillation (150 bpm) of unknown date, with nonspecific repolarization alterations. A first echocardiogram showed a non-dilated left ventricle (LV) with severely depressed ejection fraction (LVEF) of about 20%, characterized by diffuse hypokinesia. Laboratory findings showed a slight increase in myocardial necrosis markers without a significant curve, leucocytosis along with signs of acute renal and hepatic failure, and acidosis with lactate increasing.

The patient was immediately referred to the Cath lab and underwent coronary angiography that excluded significant coronary disease. Suspecting an acute myocarditis, an intra-aortic balloon pump (IABP) was positioned, with a sudden mild improvement in hemodynamic conditions, mean blood pressure and urine output. Acute renal failure was managed with a transient dialytic support. The patient, on the first day, developed a coagulopathy characterized by spontaneous INR increasing, fibrinogen and anti-thrombin III reduction, severe platelet reduction and bilirubin increase, both direct and indirect, consistent with intravascular disseminated coagulation. Massive melena developed, requiring red blood cells transfusion. The coagulopathy was treated with plasma and platelet transfusion for 10 days, and a progressive normalization was finally noted. At the same time, hemodynamic condition progressively improved: IABP was removed on the third day, LVEF progressively recovered until reaching 50% ten days after the acute presentation. AF was treated with rate control and oral anticoagulation, due to the documentation of a large LV apical thrombus. During the management of acute complications, the geneticist suggested a clinical diagnosis of Neurofibromatosis type 1 (based on café-au-lait spots, small skin fibromas, axillary and inguinal freckling).

However, despite normalization of coagulation parameters, renal function and LVEF, high levels of direct bilirubin persisted, and patient developed sub-icterus. An abdominal echo scan was then performed, identifying dilated biliary ducts, without hepatic masses or alterations; kidneys were normal, but a right adrenal incidentaloma was discovered. To confirm the diagnosis for biliary tract pathology, an MRI diagnosed the presence of an ampulloma (20 mm) but it also evidenced left (6 mm) and right (40 mm) masses of adrenal glands (Figures 1, 2 and 3). High concentrations of urine and plasma free metanephrines (p-normetanephrines: 1518 and 2480 pmol/L, p-metanephrines: 3313 and 4222 pmol/L, u24h-normetanephrines: 437 and 509 mcg/die, u24h-metanephrines: 1386 and 1830 mcg/die), high Chromogranin A (>1100 ng/mL) and neuron specific enolase (19.6 ng/mL) levels suggested the diagnosis of pheochromocytoma (PCC). The presence of distant metastasis was excluded with brain-neck-thoracic CT scan and with 123I-MIBG and 111In-Pentetreotide Scintigraphies. Both imaging methods showed surprisingly a more intense tracers’ uptake from left PCC without visualizing the ampulloma.

molecular-genetic-medicine-muscular-invasion

Figure 1: MRI image of 20 mm ampulloma (Pathological examination: Neuroendocrine tumor, G2 with muscular invasion – pT2 N0 M0).

molecular-genetic-medicine-MRI-image

Figure 2: MRI image of right 40 mm PCC (Pathological examination: Ki67 is 2%).

molecular-genetic-medicine-nuclear-pleomorphism

Figure 3: MRI image of left 6 mm PCC (Pathological examination: Vascular invasion, profound nuclear pleomorphism, mitosis 6x 10 HPF, Ki67 is 9%).

All tumors were surgically removed without complications. Pathologist confirmed the diagnosis of bilateral PCC (right adrenal gland: PCC of 40 mm, Ki67 is 2%; left adrenal gland: PCC of 5 mm with vascular invasion, profound nuclear pleomorphism, mitosis 6x 10 HPF, Ki67 is 9%) and of ampullary neuroendocrine tumor (G2 with muscular invasion – pT2 N0 M0). Results from genetic analysis confirmed the mutation in NF-1 gene. After 3 year of regular followup, the patient presents good clinical conditions and has neither biochemical nor radiological evidence of disease recurrence.

Discussion

The present case describes a rare case of bilateral PCC in NF- 1, presenting with acute heart failure and cardiogenic shock. It is important to early recognize this tumor to reduce related cardiovascular morbidity/mortality, prevent growth and extension into adjacent tissues, development of metastases and address syndromic forms. In our case, because of the clinical presentation, all diagnostic exams were directed towards acute myocarditis. The patient required hemodynamic support. Renal and hepatic failure, along with coagulopathy and melena, were considered as consequences of the cardiogenic shock.

Medical approach to PCC heterogeneous biochemical, pathological and clinical presentations is an example of precision medicine [2,3]. Genetic testing is a crucial moment of the PPGL management. In this case, the diagnosis of PCC and therefore the appropriate surgical treatment was established only after few weeks, when the patients, after recovering from the acute phase, presented persistent altered hepatic function, along with new diagnosis of hypertension. A prompt diagnosis could have directed the treatment properly in a faster time interval, avoiding time and diagnostic exams.

Some previous case reports described an acute presentation of PCC as a Tako-Tsubo-like cardiomyopathy sometimes accompanied by acute heart failure and cardiogenic shock [5-7]. However, in these series, patients presented with chest pain before symptoms of heart failure, not present in our patient. More relevant, our patient did not present ECG and echocardiographic features usually described in Tako-Tsubo cardiomyopathy, not only primary but also PCC-related. This original and myocarditis-mimicking presentation has already been reported among patients with PCC in single case reports [8-10]. Following these reports, PCC has been described as a possible cause of Tako-Tsubo cardiomyopathy, due to the effect of adrenergic stress deriving from massive catecholamine release from the tumor [11].

In the present case, PCC didn’t mimic a typical or inverted Tako- Tsubo cardiomyopathy but presented similarly to an acute fulminant myocarditis [12]. The high inflammatory markers were consistent with this presentation. However, the patient didn’t experience fever or chest pain. In this case, the diagnostic work-up was driven by the persistence of elevated cholestasis indices, suggesting an abdominal disease. In fact, PCC was identified through diagnostic exams performed to define the nature of the biliary duct mass. We discuss a very rare case. In fact, bilateral PCC occurs only in 0.6% of patients with NF-1 [13].

Conclusion

Ampullary NET is a further clinical manifestation of the syndrome. PPGLs should be quickly considered in patients with unexplained left ventricular failure, multi-or-gan failure, hypertensive crises, shock and without coronary artery disease. The diagnosis of PPGL is commonly based on measurements of metanephrines in plasma or urine. Waiting for diagnostic test results may delay rapid decisions on patient management or therapeutic interventions. The acute emergency situation is the only exception to the rule where imaging studies to search for a PPGL may be undertaken without biochemical evidence of a catecholamine producing tumour.

Conflict of Interest

The authors report no conflict of interest in this work.

References

Citation: Parasiliti-Caprino M, Matta M, Lopez C, Barbero U, Maletta F, et al. (2019) Unusual and Challenging Presentation of Hereditary Pheochromocytoma where Physicians Should Not Be Fooled - A Case Report. J Mol Genet Med 13: 428.

Copyright: © 2019 Parasiliti-Caprino M, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Select your language of interest to view the total content in your interested language

Post Your Comment Citation
Share This Article
Recommended Conferences
Article Usage
  • Total views: 374
  • [From(publication date): 0-0 - Nov 19, 2019]
  • Breakdown by view type
  • HTML page views: 350
  • PDF downloads: 24
Top