Mediastinal paragangliomas related to SDHx gene mutations

Abstract

Introduction

Paragangliomas (PGLs) related to hereditary syndromes are rare mediastinal tumors. Paragangliomas are caused by mutations in genes encoding subunits of succinate dehydrogenase enzyme (SDH).

Aim

To evaluate clinical, anatomical and functional characteristics of mediastinal paragangliomas related to SDHx gene mutations.

Material and methods

Retrospective analysis of 75 patients with confirmed SDHx gene mutations (24 patients with SDHB, 5 SDHC, 46 with SDHD mutations) was performed. Patients underwent evaluation using computed tomography (CT), somatostatin receptor scintigraphy (SRS) (^99mTc-[HYNIC,Tyr3]-octreotide), ¹²³I mIBG scintigraphy and urinary excretion of total methoxycatecholamines.

Results

Out of 75 patients, 16 (21%) patients (1 SDHB, 15 SDHD mutations) had 17 PGLs localized in the mediastinum. Fourteen PGLs were localized in the middle mediastinum (intrapericardial) and 3 PGLs in the posterior mediastinum. The median diameter of paragangliomas measured on the axial slice was 24.3 mm (interquartile range (IQR): 14.7–36.6), and the median volume was 2.78 ml (IQR: 0.87–16.16). Twelve out of 16 patients (75%) underwent SRS, and 11 of them (92.3%) had pathological uptake of the radiotracer. Eleven (68.75%) out of 16 patients underwent 123 I mIBG, with only 3 positive results. Symptoms of catecholamine excretion were observed in 3 patients with PGLs localized in the posterior mediastinum. All PGLs were benign except in 1 patient with the SDHB mutation and PGL detected in the posterior mediastinum, who had a metastatic disease.

Conclusions

Most mediastinal paragangliomas were related to SDHD gene mutations. They were asymptomatic, localized in the medial mediastinum, intrapericardially.

Introduction

Mediastinal paragangliomas are rare neuroendocrine tumors/neoplasms deriving from the autonomic nervous system. Paragangliomas (PGLs) may occur as sporadic tumors or be related to hereditary syndromes (at least one-third of all patients with PGLs) [1].

Most cases of familial paragangliomas are caused by mutations in the genes encoding A, B, C, D subunits of mitochondrial complex II enzyme succinate dehydrogenase (SDH) [2]. Predominantly, PGL syndromes are associated with SDHD and SDHB mutations. SDHC mutation is rare, and typically patients have benign, solitary head and neck paragangliomas [3]. SDHD mutation carriers most frequently develop multifocal head and neck paragangliomas; adrenal and extraadrenal PGLs occur less frequently [2, 4]. SDHB mutation carriers are at risk of malignant and extraadrenal abdominal and thoracic paragangliomas [4, 5].

Mediastinal paragangliomas are rare, accounting for about 2% of all paragangliomas [6].

Paragangliomas located in the medial mediastinum arise from paraganglia in the region of the cardiac plexus [7]. The PGLs localized in the proximity of the ductus arteriosus, the main pulmonary artery and its bifurcation and the adjacent aortic arch are termed “aortic body tumors, aorticopulmonary or aortopulmonary paragangliomas” [8]. Aortopulmonary paragangliomas are usually asymptomatic [9].

Less commonly, the paragangliomas are located in the posterior mediastinum and arise from the para-vertebral sympathetic chain ganglia. About 50% of posterior mediastinal paragangliomas are functional [10].

Symptoms of paragangliomas usually are associated with mass effect or hypersecretion of catecholamines. Clinical symptoms related to catecholamine hypersecretion include hypertension, headaches, palpitations, and sweating. The biochemical diagnosis is based on demonstration of an increased level of catecholamine metabolites in plasma and/or urine [1, 4, 5].

Some reports have suggested that mediastinal paragangliomas often have an aggressive course and patients should be carefully followed up [6, 11].

Surgical treatment is considered to be the gold standard in the treatment of thoracic paragangliomas [12], but it may be a challenge. Precise information about localization and relation to other anatomical structures is required before taking the treatment decision.

Paraganglioma diagnosis is based on anatomical and functional examinations. Computed tomography (CT) and magnetic resonance imaging (MRI) are used as anatomical methods and ¹²³I-metaiodobenzylguanidine scintigraphy (mIBG) and somatostatin receptor scintigraphy (SRS) as functional methods in the detection of paragangliomas [13–15].

Aim

The aim of the study was to evaluate clinical, biochemical and imaging characteristics of mediastinal paragangliomas related to SDHx gene mutations.

Material and methods

We retrospectively analyzed the patients with SDHx mutations confirmed by genetic testing and registered in the Polish Pheochromocytoma-Paraganglioma Registry. Carriers of SDHx germline mutations (both index cases and their relatives) underwent evaluation of the head and neck, the thorax, the abdomen and the pelvis using computed tomography (CT) and the level of daily urinary excretion of total methoxycatecholamines was determined.

The protocol for this study was approved by the local ethics committee. Exclusion criteria were a refusal or inability to understand or sign the informed consent, contraindications to administer iodate contrast material, being pregnant or lactating women. All patients signed the informed consent before participating in the study.

Overall, 75 patients were enrolled in the study (24 patients with SDHB mutations, 5 with SDHC, 46 with SDHD mutations); 16 patients had PGLs localized in the mediastinum. The CT examinations were performed using a dual source scanner (Somatom Definition, Somatom Definition Flash, Siemens Medical Solutions, Erlangen, Germany) after contrast administration.

The slice thickness was 1 mm, tube voltage was set at 80–120 kV, tube current 165–210 mA, depending on scanning regions and body size.

Highly iodinated contrast material (≥ 350 mg/ml) was administered in the antecubital vein in the amount of 80–100 ml (depending on the body size) at a flow rate of 4–5 ml/s. The scans were done in the arterial phase 30 s after contrast injection. The images were reconstructed with a standard soft-tissue-kernel algorithm.

Six out of 16 patients underwent CT examinations outside our department before the surgery.

A well-defined soft tissue mass with typical high enhancement after i.v. contrast agent administration was recognized as a paraganglioma [16]. Based on CT examinations, localization of paragangliomas, relation to other anatomical structures, invasion of the adjacent structures, their dimension and volume were analyzed.

Mediastinal paragangliomas were divided into tumors localized in the anterior, middle or posterior mediastinum. Paragangliomas associated with the heart were classified as intrapericardial or intracardiac PGLs.

According to the World Health Organization, the criterion for the diagnosis of malignant pheochromocytoma or PGL was the presence of metastases [17].

Carriers of the SDHx gene mutations with paragangliomas detected by CT examination were subsequently screened by somatostatin receptor scintigraphy (SRS) and mIBG scintigraphy as additional functional imaging modalities.

SRS was performed using ^99mTc-[HYNIC,Tyr3]-octreotide ^99mTc [TOC] (600-700 MBq) (Tektrotyd; National Center For Nuclear Research-Polatom; Poland). The detailed method of kit labeling with ^99mTc was presented previously [18]. Images were acquired between 1 and 3 hours after the i.v. injection of a radiotracer using a double-head camera. The acquisition of head, neck, chest, abdominal and pelvis images was performed using the whole-body single photon emission computed tomography (WB-SPECT) method.

A ¹²³I mIBG (AdreView, GE Healthcare; USA) study was performed in 11 patients. In each case after thyroid suppression using Lugol's solution, one day before the study, the patients received an injection of 300–370 MBq of ¹²³I mIBG. Images were acquired between 18 and 22 hours after the i.v. injection of the radiotracer using a double-head camera. The acquisition of head, neck, chest, abdominal and pelvis images was performed using the same method as with SRS – whole-body SPECT.

As with SRS, any focal or diffuse nonphysiological accumulation observed during the examination was reported as pathological. Diffuse low-activity intestinal uptake (with SRS) or liver and heart uptake (with mIBG) was rated as nonspecific, physiologic uptake.

Statistical analysis

Due to the non-normal distribution of most data, the results are presented as median and interquartile range (IQR). Frequency and percentages were reported for categorical variables. Statistical analysis was performed using IBM SPSS 20 for Linux (IBM SPSS Inc, Chicago, IL; USA).

Results

Out of 75 patients, 16 (21%) patients (15 SDHD, 1 SDHB) had paragangliomas localized in the mediastinum. Altogether 207 paragangliomas were detected in different regions, 17 (8.2%) of which were localized in the mediastinum.

All patients with SDHD mutations, except 1, had a C11X nonsense mutation, which was recognized as a founding mutation [17], and 1 patient had an exon deletion. In 1 SDHB carrier, we observed a missense mutation.

The median age was 37 years (IQR: 28.25–46.75). The male to female ratio was 1 : 1.

One patient with SDHB mutation had a malignant disease with metastasis to the lung, bone and lymph nodes. Table I contains patients’ characteristics and tumor localizations.

Tab. I.

Characteristics of patients and localizations of tumors

Patient no.	Gender	Age [years]	Gene	Mutation type	Thoracic PGL found at initial diagnosis	Tumor location	Tumor size [cm] on CT	Surgical resection	Multifocal PGLs	SRS 99mTc [TOC] SPECT	123I mIBG* SPECT	Malignant
1	F	48	SDHD	Exon 1, c.33C > A, p. C11X Nonsense	No	Posterior mediastinum Th2–Th3	2 × 2.3	Yes	Yes HNP, pheo, abdomen extraadrenal	Positive	Positive	No
2	F	43	SDHD	Exon 1 deletion	No	Middle mediastinum (between LA, right pulmonary artery, ascending aorta)	4.5 × 3.5	Yes	Yes Abdomen Extraadrenal	Positive	Positive	No
3	M	30	SDHD	Exon 1, c.33C > A, p. C11X Nonsense	No	Middle mediastinum (between aortic root, pulmonary trunk and LAD)	1.6 × 1.3	No	Yes HNP, pheo	Positive	Negative	No
4	F	39	SDHD	Exon 1, c.33C > A, p. C11X Nonsense	No	Middle mediastinum (between aortic root, pulmonary trunk and LAD)	1.3 × 1.2	No	Yes HNP, pheo, Abdomen Extraadrenal	Positive	Negative	No
5	M	59	SDHD	Exon 1, c.33C > A, p. C11X Nonsense	No	Middle mediastinum (aortopulmonary window)	2.1 × 1.8	No	Yes HNP	Positive	Negative	No
6	F	40	SDHD	Exon 1, c.33C > A, p. C11X Nonsense	No	Middle mediastinum (between LA and descending aorta)	3.7 × 2.0	Yes	Yes HNP, abdomen extraadrenal	Positive	ND	No
7	F	34	SDHD	Exon 1, c.33C > A, p. C11X Nonsense	No	Middle mediastinum (between right pulmonary artery and LA) Middle mediastinum (aortopulmonary window)	1 × 1.1 2.7 × 3.5	Yes Yes	Yes HNP, abdomen extraadrenal	Positive Positive	Negative Negative	No
8	M	33	SDHD	Exon 1, c.33C > A, p. C11X Nonsense	No	Middle mediastinum (aortopulmonary window)	2.5 × 1.7	No	Yes HNP, pheo	Positive	Negative	No
9	M	64	SDHD	Exon 1, c.33C > A, p. C11X Nonsense	No	Middle mediastinum (between VCS, ascending aorta, right pulmonary artery and trachea)	3 × 2	Yes	Yes HNP	ND	ND	No
10	M	28	SDHD	Exon 1, c.33C > A, p. C11X Nonsense	No	Middle mediastinum (aortic pulmonary window)	1.5 × 1.6	No	Yes HNP	Positive	Negative	No
11	M	26	SDHD	Exon 1, c.33C > A, p. C11X Nonsense	No	Middle mediastinum (right atrioventricular groove near RCA)	3.6 × 2.3	No	Yes HNP	Positive	Negative	No
12	F	30	SDHD	Exon 1, c.33C > A, p. C11X Nonsense	No	Posterior mediastinum	N	Yes	Yes HNP, abdomen extraadrenal	ND	ND	No
13	F	33	SDHD	Exon 1, c.33C > A, p. C11X	No	Middle mediastinum (aortopulmonarywindow)	0.7 × 0.6	No	Yes HNP	Negative	Negative	No
14	F	52	SDHD	Exon 1, c.33C > A, p. C11X Nonsense	??	Middle mediastinum (between aortic arch, right pulmonary artery, VCS, trachea)	5.2 × 4.7	Yes	Yes HNP	ND	ND	No
15	M	22	SDHB	Exon 6, c.708T > C (int. 574 T > C), p. C192R Missense	Yes	Posterior mediastinum Th8–Th11	N	Yes	Yes HNP	Positive	Positive	Yes
16	M	40	SDHD	Exon 1, c.33C > A, p. C11X Nonsense	No	Middle mediastinum (between aortic bulb, LAD and LA)	3.5 × 2	No	Yes HNP	ND	ND	No

ND – not done, VCS – venae cave superior, LA – left atrium, LAD – left descending artery, RCA – right coronary artery, HNP – head and neck paraganglioma, pheo – pheochromocytoma, N – no data are available, only histological outcome

Localization of paragangliomas

Fourteen paragangliomas were localized in the middle mediastinum and 3 PGLs in the posterior mediastinum. None of the PGLs was localized in the anterior mediastinum.

All medial mediastinal paragangliomas were localized intrapericardially; no paragangliomas had an intracardiac localization. Five paragangliomas were localized in the aortopulmonary window (Figs. 1 A, B), and in 4 cases paragangliomas were localized in the proximity of the coronary arteries (3 close to the left descending artery, 1 close to the right coronary artery) (Figs. 2, 3). A single paraganglioma was localized near the aortic arch, 2 between the left atrium and the right pulmonary artery (Figs. 4 A, B) and 2 among the vena cava superior (VCS), the ascending aorta and the trachea. We did not observe any signs of PGL invasion of the adjacent structures.

Fig. 1.

Contrast-enhanced chest CT, multiplanar reconstruction (MPR): A – coronal view, B – sagittal view. Images show a hypervascular tumor in the aortopulmonary window (arrows)

Fig. 2.

Contrast-enhanced chest CT, maximum intensity projection (MIP) coronal view shows a hypervascular tumor located near the left descending artery (LAD) (arrow)

Fig. 3.

Cardiac CT angiography, multiplanar reconstruction (MPR) axial view shows a hypervascular tumor located in the right atrioventricular groove (arrow)

RA – right atrium, RV – right ventricle

Fig. 4.

Contrast-enhanced chest CT, multiplanar reconstruction (MPR), A – axial view, B – coronal view, shows a mediastinal tumor adjacent to the ascending aorta, left atrium (LA), vena cava superior and right pulmonary artery (RPA) (arrows)

The median diameter of paragangliomas measured on the axial slice was 24.3 mm (IQR: 14.7–36.6), and the median volume was 2.78 ml (IQR: 0.87–16.16).

The arterial phase images obtained in 14/17 paragangliomas showed a median tumor attenuation of 165 HU (IQR: 141–187).

Twelve (75%) out of 16 patients underwent SRS, 11 of whom (92.3%) had pathological uptake of the radiotracer in the mediastinal PGLs.

Eleven (68.75%) out of 16 patients underwent ¹²³ I mIBG, with only 3 positive results in mediastinal PGLs.

All patients had multifocal paragangliomas, 14/16 were localized in the head and neck region, 6/16 extraadrenal PGLs were localized in the abdomen, and 4 patients had a history of pheochromocytomas.

Symptoms

Symptoms of catecholamine excess were present in only 3 patients, with paragangliomas localized in the posterior mediastinum, and after surgical treatment the level of catecholamines was normal. All patients with middle mediastinum tumors were asymptomatic.

Treatment

Eight (50%) patients underwent surgical treatment, 5 patients with paragangliomas localized in the middle mediastinum (1 patient had surgical resection of 2 mediastinal paragangliomas) and 3 patients with PGLs localized in the posterior mediastinum. Three patients with PGLs localized in the middle mediastinum required subsequent surgery due to intraoperative complications of the tumor resection. None of the patients died due to intra- or postoperative complications.

One patient with a middle mediastinum PGL underwent surgery with additional radiotherapy. All resected tumors were confirmed in histopathological examinations as paragangliomas. Remaining patients (50%) were treated conservatively.

Follow-up

All the patients who underwent surgery were followed up with CT. The median follow-up was 50 months (range: 24–204 months). During the follow-up, none of the surgically treated patients had a residual tumor or developed metastatic diseases. One SDHB gene mutation carrier had a metastatic disease at the time of the diagnosis of a posterior mediastinal paraganglioma.

Eight patients treated conservatively underwent follow-up examinations.

The median follow-up was 61 months (range: 13–74 months). None of the conservatively treated patients developed metastatic diseases.

Discussion

Paragangliomas related to SDHx gene mutations are mainly localized in the head and neck region, and extraadrenally in the abdomen [18–20]. The mediastinum is a rare localization of paragangliomas; only 2% of all PGLs are found there [6]. The largest studies of mediastinal paragangliomas were based on the Mayo Clinic experience (14 patients) and the report of Martucci et al. (a multi-institutional study that included 15 patients) [21, 22]. Their findings similar to Ghayee underline that mediastinal paragangliomas are closely related to SDHx mutations and are often malignant [6].

Importantly, most patients in those reports had symptoms associated with catecholamine hypersecretion or cardiac-related symptoms of chest pain and/or shortness of breath [21, 22].

Nowadays due to extensive use of diagnostic chest imaging, some paragangliomas are diagnosed incidentally.

Furthermore, genetic counseling recommended to PGL families and the subsequent screening of carriers by anatomical imaging techniques have led to the detection of small paragangliomas, which can be localized in the mediastinum.

Our study represents a different group of patients with mediastinal paragangliomas than that in previous reports [21, 22]. All patients were carriers of SDHx mutations, and the majority of our patients underwent a CT evaluation of the chest as a screening test after detecting SDHx gene mutations.

We found that the prevalence of mediastinal PGLs may be higher in carriers of SDHx mutations than previously reported [6], especially in SDHD gene mutations. However, the majority of patients were asymptomatic.

Among 75 patients with SDHx gene mutations, 16 (21%) patients had paragangliomas located in the mediastinum, but only 3 patients (with paragangliomas located in the posterior mediastinum) had symptoms associated with catecholamine hypersecretion, while the remaining patients were asymptomatic.

Surgical treatment remains a preferred method of treatment for paragangliomas.

Complete resection of the tumors is demanding due to their highly vascular nature and anatomical position, especially the proximity to major vessels or coronary arteries [11]. Surgical resection is often complicated by excessive hemorrhage and reconstruction of the surrounding structures [23]. In cases of a paraganglioma invasion into the heart, coronary arteries or other great vessels, a cardiopulmonary bypass should be employed [21]. A careful preoperative assessment of the tumor location is crucial and determines the surgical approach. Incomplete resection and high perioperative mortality (5.3% to 9%) have been reported [8, 24]. Using ECG gated CT in patients with suspected PGL located intracardially or intrapericardially significantly improves the image quality [22].

Paragangliomas located in head and neck regions are slowly growing tumors [25], and mediastinal paragangliomas seem to be slowly growing too.

In chosen cases when a tumor is asymptomatic and surgical treatment is not an option due to its location, conservative treatment and follow-up may be considered.

In our report, the prevalence of mediastinal paragangliomas was higher (8.2%) than in other reports, mainly due to SDHD gene mutations and with a benign course [6]. None of the conservatively or surgically treated patients developed metastatic diseases. Only one SDHB carrier had a malignant PGL.

It should be emphasized that almost all of our SDHD patients harbor one type of mutation. It is SDHD p.C11X, which was recognized as a Polish founder mutation [16]. The high frequency of mediastinal tumors in our group may de facto reflect the risk profile of that particular mutation.

Conclusions

Most mediastinal paragangliomas were related to SDHD gene mutations, were asymptomatic, and were localized intrapericardially. None of the PGLs related to SDHD mutations were malignant, and during the follow-up no metastases were detected.

Mediastinal PGLs were associated with other localizations, mainly in the head and neck region. Only one mediastinal PGL related to SDHB mutation was malignant.

The results of our study show that the prevalence of mediastinal paragangliomas in asymptomatic SDHx mutation carriers may be higher than previously believed.

Funding

This work was supported by a grant from the Institute of Cardiology in Warsaw, Poland (grant no. 2.4/II/14).

Biography

Disclosure

Authors report no conflict of interest.