- Case report
- Open Access
Paraganglioma of the greater omentum: Case report and review of the literature
© Archontovasilis et al; licensee BioMed Central Ltd. 2007
- Received: 23 January 2007
- Accepted: 03 August 2007
- Published: 03 August 2007
Extra-adrenal, intra-abdominal paraganglioma constitutes a rare neoplasm and, moreover, its location in the greater omentum is extremely infrequent.
A 46-year-old woman with an unremarkable medical history presented with an asymptomatic greater omentum mass that was discovered incidentally during ultrasonographic evaluation due to menstrual disturbances. Clinical examination revealed a mobile, non-tender, well-circumscribed mass in the right upper and lower abdominal quadrant. Blood tests were normal. Contrast-enhanced abdominal computed tomography (CT) scan confirmed a huge (15 × 15 cm), well-demarcated, solid and cystic, heterogeneously enhanced mass between the right liver lobe and right kidney. Exploratory laparotomy revealed a large mass in the greater omentum. The tumor was completely excised along with the greater omentum. Histopathology offered the diagnosis of benign greater omentum paraganglioma. After an uneventful postoperative course, the patient was discharged on the 4th postoperative day. She remains free of disease for 2 years as appears on repeated CT scans as well as magnetic resonance imaging (MRI) and scintigraphy performed with radiotracer-labeled metaiodobenzyl-guanidine (MIBG) scans.
This is the second reported case of greater omentum paraganglioma. Clinical and imaging data of patients with extra-adrenal, intra-abdominal paragangliomas are variable while many of them may be asymptomatic even when the lesion is quite large. Thorough histopathologic evaluation is imperative for diagnosis and radical excision is the treatment of choice. Since there are no definite microscopic criteria for the distinction between benign and malignant tumors, prolonged follow-up is necessary.
- Multiple Endocrine Neoplasia Type
- Vasoactive Intestinal Polypeptide
- Great Omentum
- hTERT Expression
Extra-adrenal paragangliomas of the sympathoadrenal neuroendocrine system consist 5%–15% of sporadic pheochromocytomas and are located anywhere extending from the upper neck to the pelvic floor, parallel to the autonomic nervous system [1, 2]. Extra-adrenal, abdominal paragangliomas are divided into three groups: superior para-aortic, inferior para-aortic, and urinary bladder tumors . Rarely, extra-adrenal paragangliomas can occur aberrantly outside this distribution. The annual worldwide incidence of paragangliomas, as well as in Greece, is approximately 1/300,000 [3, 4].
Herein, we report such a case of a paraganglioma occurring in the greater omentum in a 46-year-old woman along with a review of the literature. To the best of our knowledge, this is the second reported case of greater omentum paraganglioma in the literature . Apart from its extremely infrequent location, the reported case is important because of the rather huge diameter of the tumor and the asymptomatic course of the patient prior to diagnosis as well as the characteristic radiological and pathological figures that are presented.
Due to histopathologic diagnosis, genetic testing for familial paraganglioma, neurofibromatosis type 1, von Hippel-Lindau disease, the Carney triad, multiple endocrine neoplasia type 2, and mutations of the succinate dehydrogenase genes (SDHB, SDHC, and SDHD) was performed that was negative.
After an uneventful postoperative course, the patient was discharged on the 4th postoperative day. She remains free of disease for 2 years as appears from repeated biochemical testing (plasma catecholamines, plasma-free metanephrines, urinary catecholamines, urinary vanillylmandelic acid, urinary total metanephrines, urinary fractionated metanephrines), CT scans as well as magnetic resonance imaging (MRI) and scintigraphy performed with radiotracer-labeled metaiodobenzyl-guanidine (MIBG) scans.
The paraganglion system is formed by numerous collections of neuroepithelial cells. Their common morphologic characteristic is the presence of numerous cytoplasmic neurosecretory granules containing catecholamines. Paraganglioma is the generic term applied to tumors of paraganglia regardless of location. Paragangliomas of the adrenal medulla, the most common site of paragangliomas, are known as pheochromocytomas while those located outside the adrenal gland as extra-adrenal pheochromocytomas .
Extra-adrenal paraganglia are divided into two categories: those related to the parasympathetic system and those connected with the orthosympathetic system. The former, usually nonchromaffin, lie in the head and neck including the carotid body, intravagal, jugulotympanic, and mediastinal and aorticopulmonary paraganglia [7, 8]. The latter are chromaffin, associated with the peripheral sympathetic nervous system, and secrete catecholamines in response to sympathetic neural stimulation. They lie in the paraaxial region of the trunk close to the paravertebral and prevertebral ganglia or in the connective tissue adjacent to pelvic organs, predominating along the thoracolumbar paraaortic region in the retroperitoneum [9, 10]. The adrenal medulla and the organs of Zuckerkandl are the only ones visible to the naked eye [6, 10].
Extra-adrenal, intra-abdominal paragangliomas are divided into three groups: superior para-aortic, inferior para-aortic, and urinary bladder paragangliomas [9, 11]. Rarely, paragangliomas have been described in other unusual sites, such as the gallbladder , mesentery , kidney , prostate , and ovary . We hypothesize that the paraganglioma in our patient was derived from the paraganglionic cells by vertebral migration from the root of superior mesenteric artery. The development of a paraganglioma in the greater omentum is extremely rare and this case represents the second report in the literature . As with other paragangliomas described outside the distribution of paraganglionic tissue, our case may be explained by the migration patterns of the widely dispersed neural crest cells.
Paragangliomas may be hereditary and can be associated with familial paraganglioma, neurofibromatosis type 1, von Hippel-Lindau disease, the Carney triad, multiple endocrine neoplasia type 2, and mutations of the succinate dehydrogenase genes (SDHB, SDHC, and SDHD) . Genetic testing should, therefore, be considered in all patients with paraganglioma. In the presented case, genetic testing was performed and was negative.
Histologically, paraganglia contain nests of neuroendocrine cells surrounded by sustenacular cells. This pattern is most clearly seen in parasympathetic paraganglia as the characteristic "zellballen". In sympathetic paraganglia, neuroendocrine cells are referred to as chromaffin cells and in parasympathetic as chief cells. These cells are immunopositive for neuroendocrine markers including synaptophysin and chromogranin A and for several neuropeptides. Features that may predict malignancy include extra-adrenal location, confluent tumor necrosis, vascular invasion, local invasion, coarse nodularity, and absence of hyaline globules . Moreover, decreased expression of neuropeptides and, particularly, negative staining for enkephalins, somatostatin, pancreatic polypeptide, and VIP have been associated with malignancy . Although the presented tumor was extra-adrenal, the presence of hyaline globules and the absence of confluent tumor necrosis, vascular invasion, local invasion, and coarse nodularity along with the positive staining for the above-mentioned polypeptides show the benign nature of this lesion.
Most patients with extra-adrenal, abdominal paragangliomas present with abdominal pain or a palpable abdominal mass ; however, they may be asymptomatic even when the lesion is large and the tumor is incidentally found during radiographic evaluation for other reasons, such as the presented patient. Other symptoms may be nausea, vomiting, diarrhea, abdominal distension, and weight loss. Increased catecholamine secretion in functional tumors is responsible for symptoms such as hypertension, flashing, sweating, headache, diaphoresis, anxiety, tachycardia, or palpitations [9, 11, 19].
Even though imaging studies are helpful, diagnosis of extra-adrenal, intra-abdominal paragangliomas can be safely done only with careful histologic and immunohistochemical evaluation. Contrast-enhanced abdominal CT scan is useful for diagnosis; however, no CT feature unique for paragangliomas has been found . Abdominal MRI and MIBG are essential in localization and characterization of paragangliomas while MRI has the highest sensitivity in detection of extra-adrenal paragangliomas as well as pheochromocytomas [20, 21].
The majority of abdominal tumors are benign; 10%–50% of intra-abdominal, extra-adrenal paragangliomas are reported to be malignant [9–11, 19, 22]. Malignant forms frequently develop distant metastases in lung, liver, and lymph nodes. Annual postoperative biochemical testing (plasma catecholamines, plasma-free metanephrines, urinary catecholamines, urinary vanillylmandelic acid, urinary total metanephrines, and urinary fractionated metanephrines), CT scans as well as MRI and MIBG scans are essential for assessment for metastatic disease, tumor recurrence or delayed appearance of multiple primary tumors .
Clinical and histological distinction between benign and malignant cases is difficult [9, 23, 24]. The only proof of malignancy is the presence of metastases or local invasion while in localized tumors there are no absolute criteria for predicting malignant potential. This principle has the drawback that some cases will initially be classified as benign and then reclassified as malignant if metastases are identified at follow-up. There is, therefore, a clear need for additional diagnostic tools to enable detection of malignant cases at initial surgery. Additional diagnostic markers would be valuable, but, up to date, no reliable prognostic markers have been identified [23, 24]. Although several markers such as immunohistochemical expression of the cell proliferation marker Ki-67/MIB-1, telomerase activity, hTERT expression, topoisomerase IIa expression, and mRNA expression of MMP-2 and EMMPRIN metalloproteinases have shown promising results, they need further evaluation. Even though these markers seem to be very valuable, particularly when combined with histopathology, no single test or combination of tests has yielded sufficiently high sensitivity and specificity to result in widespread acceptance in everyday clinical practice [22–26]. Due to the rarity of the tumor, multicenter studies are probably necessary in this effort . The very low proliferation index (<1%) found in the presented case and the fact that no telomerase activity, hTERT expression, topoisomerase IIa expression, or mRNA expression of MMP-2 and EMMPRIN metalloproteinases was identified show the benign nature of this lesion.
The treatment of choice for paragangliomas is complete surgical resection. Traditional treatment consists of open exploration and resection. However, laparoscopic management is nowadays increasingly being used for their management due to the advances in laparoscopic technique and refined preoperative imaging even though few studies regarding the laparoscopic treatment of extra-adrenal intra-abdominal paragangliomas exist in the literature because of the rarity of this clinical entity . Intraoperative ultrasound is considered an invaluable tool for laparoscopic surgeons in these cases. In these studies of laparoscopic management, encouraging results are presented; it should be mentioned, however, that all tumors were less than 4 cm . In the presented patient, due to the huge size of the tumor, laparoscopy was considered impossible and, therefore, not performed.
Since clinical presentation and imaging data of these patients are variable and non specific, histological distinction between benign and malignant cases as well as prediction of malignant potential are difficult, and local recurrence or distant metastases are not infrequent, a multidisciplinary approach regarding effective diagnosis, management and follow-up is essential and should involve the close collaboration of endocrinologists, surgeons, anesthesiologists, geneticists, laboratory specialists, radiologists, oncologists, and pathologists.
Paraganglioma of the greater omentum is extremely infrequent. Recognition of this tumor as a cause of an abdominal mass is important. Clinical and imaging data of patients with extra-adrenal, intra-abdominal paragangliomas are highly variable and non specific while many of them may be asymptomatic even when the lesion is quite large, such as the presented case. Thorough histological and immunohistochemical evaluation is, therefore, imperative and the only safe modality for diagnosis. The first line treatment is surgical resection, while chemotherapy and radiotherapy seem to be useless in benign lesions [19, 22]. Since there are no definite microscopic criteria for the distinction between benign and malignant tumors, radical excision is the treatment of choice and prolonged follow-up is necessary.
Written consent was obtained from the patient for publication of this case report.
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