Robotic excision of interaortocaval paraganglioma: a case report with the literature review

Abstract

Background

Paragangliomas are rare neuroendocrine tumors of extra adrenal origin. The symptomatic paragangliomas require multimodal treatment approach.

Case Presentation

We report a case of 34-year-old female who presented with complains of headache and blurring of vision. Examination revealed Hypertensive crisis with grade 3 retinopathy. The patient was diagnosed as a case of extra-adrenal paraganglioma during evaluation for secondary hypertension. Magnetic Resonance Imaging of the abdomen revealed 23*28*28 mm mass lesion in the inter-aortocaval region at the level of L3–L4. The patient was started on medical management for hypertension and was managed safely with robot-assisted surgery, owing to enhanced visualization of feeding vessels and avoidance of excessive manipulation of tumor.

Conclusions

Our case report emphasizes on the robot assisted surgical technique for the removal of tumor in a vulnerable anatomical position and presents a review of the literature.

1 Background

Extra-adrenal pheochromocytoma are called Paraganglioma (PPGLs). They arise from chromaffin tissue derived from primitive neuroectoderm. Some are asymptomatic and some present with adrenergic symptoms due to release of catecholamines. Symptomatic paraganglioma are usually managed with surgical resection. Minimal invasive techniques are used recently in management of these tumors, we report a case of Interaortocaval paraganglioma managed with Robotic excision.

2 Case presentation

34-year-old female presented with complains of headache, blurring of vision and excessive sweating of 4 months duration. She denied any history of vomiting, syncope, chest pain breathlessness, oliguria, altered sensorium, neurological deficit, menstrual irregularity, weight loss or altered bowel habits. There was no significant medical/surgical history in the past. General examination revealed BP—200/130 mmHg, PR—72/min. Fundoscopy—Grade 3 hypertensive retinopathy. Rest systemic examination was unremarkable. Patient was started on antihypertensives and evaluated further as case of secondary hypertension. Baseline hematological, biochemistry workup and thyroid profile were normal. Twenty-four h urinary Metanephrines—1306mcg (normal—< 600mcg) and Normetaphrines—1332mcg (normal—23–105 mcg). Doppler of renal vessels was normal. Magnetic Resonance imaging (MRI) abdomen showed 23*28*28 mm well defined smoothly marginated mass lesion in the inter Aortocaval region at level of L3–4, abutting 3rd part of duodenum and pancreas. The mass lesion was homogenously hyperintense on T2W1, hypointense on T1W1 and showed peripheral rim enhancement on post contrast images (Fig. 1). ¹³¹I-metaiodobenzylguanidine (MIBG) scan showed faint avidity suggesting tumor of neural crest origin. The diagnosis of interaortocaval paraganglioma was made and subsequently robotic excision was planned. She was started on preoperative preparation with good hydration, started on alpha blockers, Angiotensin-Converting Enzyme inhibitors and calcium channel blockers; beta blockers were started after 1 week of alpha blockers.

Fig. 1

a Coronal section of Magnetic resonance imaging (MRI) showing 2.3 × 2.8 × 2.8 cms well defined smoothly marginated mass lesion in the inter Aortocaval region at level of L3–L4 vertebra. b Axial section showing lesion is Hypointense on T1 weighted images. c Sagittal section showing lesion homogenously hyperintense on T2 weighted images. d Axial section showing peripheral rim enhancement and heterogenous central enhancement on post contrast images

3 Surgery

Patient was placed in left lateral position under General Anesthesia. Pneumoperitoneum was created, 12 mm camera port was placed in supra-umbilical location. 5 mm robotic ports were placed in epigastric, right hypochondrium and right iliac region in spino-umbilical line. 2 assistant ports were placed triangulating the robotic ports for suctioning, irrigation and clip application. Medial mobilization of right colon done; hepatic flexure was dissected; duodenum was kocherized. Tumor bulge was identified; on further dissection IVC was identified; gonadal vein was inadvertently injured and ligated. The attachments around the tumor were carefully dissected; 2 vein tributaries draining to IVC were identified and clipped. Solitary arterial supply arising from aorta was identified and clipped (Fig. 2) Tumor was extracted into endocatch bag and removed. Intraoperative blood loss was 50 ml and total time of surgery was 150 min. During the procedure, BP was stable with minimal fluctuations (150–200 mmHg) during handling of the tumor were noted. Postoperatively, patient was monitored in intensive care overnight and was shifted to the postoperative ward the following day. Abdominal drain was removed on 2nd postoperative day and patient was discharged on single antihypertensive. Final histopathology showed paraganglioma showing immunopositivity with chromogranin and synaptophysin (Fig. 3). After 1 month, her antihypertensive was stopped and urinary catecholamines showed normal levels. Follow-up after 1 year of surgery, patient was asymptomatic, normotensive with no evidence of relapse or recurrence on MIBG scan and normal urinary catecholamines levels.

Fig. 2

a Tumor bulge identified after colon mobilization and kocherization of duodenum. b Clipping and division of venous tributary. c Solitary arterial supply clipped. d Final removal of specimen

Fig. 3

Microphotographs of H & E stained sections of show an encapsulated lesion with underlying zellballen pattern (star) separated by segmented bands of prominent fibrovascular network (a 40×, b 100×). These large polygonal cells have abundant granular eosinophilic cytoplasm and central nuclei with mild nuclear atypia. Tumor cells show cytoplasmic immunopositivity for chromogranin (c) and synaptophysin (d)

4 Discussion

Pheochromocytomas are rare, catecholamine-secreting tumor with annual incidence in general population is approximately 0.6–0.8 cases per 100,000 person-years [1]. It most commonly arises from adrenal medulla, and 1–25% of the tumors are found in extra-adrenal sites which are termed paraganglioma. The embryological development of paragangliomas occurs from chromaffin cells in the preaortic paravertebral sympathetic plexus that are derivatives of neural crest cells. There are sympathetic paragangliomas that arise from sympathetic tissue and are found in abdominal region, and parasympathetic paraganglioma that arise from parasympathetic tissue and are often found in the thorax, head and neck [2]. The most common sites of paragangliomas include organ of Zuckerkandl located between aortic bifurcation and inferior mesenteric artery, carotid body, head, mediastinum and periaortic region. Majority of paragangliomas are sporadic; however, 30% are associated with familial syndromes such as Von Hippel lindau, Neurofibromatosis type 1, Multiple Endocrine Neoplasia (MEN) type 2 and carney triad [3].

Paragangliomas are usually classified as functional and nonfunctional. The symptoms of functional paraganglioma are related to catecholamine release, including paroxysmal hypertension, diaphoresis, headache, palpitations and tachycardia. Rarely- Hyperglycemia, panic attacks, fever, weight loss, myocardial infarctions, osteolytic bone metastases, and Raynaud’s phenomenon can occur [4]. They occur more often in men and usually in the 3rd or 4th decade of life. 30–40% of the paragangliomas are malignant; it is difficult to differentiate between benign and malignant histologically and malignancy is defined on basis of metastasis [5].

The diagnosis usually requires biochemical, anatomical and functional imaging. Elevated catecholamines and their metabolites (Metanephrines and Vanillylmandelic Acid) in serum and urine confirm the diagnosis [6]. Anatomical imaging with CT and MRI scans is useful in localizing the tumor. The tumor on CT scan usually appears as hypervascular masses with areas of intralesional hemorrhages and necrosis (salt and pepper appearance) [7]. CT scan have approximately 90% sensitivity for localization of extra-adrenal tumor, whereas on MRI lesion appear hyperintense on T2 weighted images and have sensitivity approximately 93–100%. Functional imaging with ¹³¹I-MIBG scintigraphy carries sensitivity of 60–80% and specificity of 95–100%. Recently used imaging techniques include Somatostatin-receptor scintigraphy, DOTATE PET and ¹⁸F FDG PET carries more sensitivity and specificity as compared to MIBG scan [8].

The definitive management of paragangliomas is surgical resection. Preoperative stabilization with fluid hydration, alpha blockade and beta blockers is critical [9]. Intraoperative hypertensive crisis during handling of tumor should be discussed with anesthetist and emergency drugs (Sodium Nitroprusside, Nitroglycerine and Esmolol) must be available for rapid control of hypertensive crisis. There are case reports available managing these tumors with minimal invasive techniques such as laparoscopy [10], we preferred robot-assisted technique owing to the difficult location of the tumor. Robot-assisted surgery has been used in few cases, there is no standard technique defined due to rarity of this condition [11, 12].

5 Conclusions

Surgical resection was successfully completed in this case due to sharp dissection, better control, and enhanced visualization provided by robotic instruments, especially in vulnerable anatomical location between IVC and aorta. Robotic surgery offered an opportunity to tackle the enlarged feeding vessels first, improved dexterity and without any manipulation of the tumor leading to better patient outcomes.