- Case report
- Open Access
Atypical glomus tumor arising in the liver: a case report
© Hirose et al. 2015
- Received: 8 May 2015
- Accepted: 9 July 2015
- Published: 19 July 2015
Glomus tumors typically occur in the subcutaneous tissue of distal extremities, but rarely in visceral organs. Most glomus tumors are benign, while others have been reported to have malignant potential. Herein, a unique case of a liver glomus tumor with atypical histological features is reported.
A 39-year-old man felt fullness in the epigastrium, and an enhanced computed tomography (CT) scan of the abdomen and pelvis revealed a 21-cm solid and cystic mass in the left liver lobe. The patient underwent a left hepatic lobectomy, and the tumor was pathologically identified as a glomus tumor with atypical histological features in the liver. This case is unique for three reasons. First, cases of glomus tumors in the liver are extremely rare. Second, this is the first report of a hepatic glomus tumor with histologically atypical features. Third, immunohistochemical staining showed focal positivity for synaptophysin. A literature review revealed that glomus tumors in visceral organs positive for synaptophysin show histological atypical features in most cases.
This is the first case of a glomus tumor with atypical histological features arising in the liver. This unique case and literature review yielded interesting findings and enabled us to postulate that synaptophysin positivity may be indicative of atypical histological features in glomus tumors arising in visceral organs.
- Glomus tumor
- Atypical features
A glomus tumor is an uncommon mesenchymal perivascular tumor considered a vascular hamartomatous derivative of glomus bodies responsible for the thermoregulation of distal extremities. Most glomus tumors are diagnosed in patients in their fourth to sixth decades of life, although symptoms are often present for several years prior to diagnosis. Radiographic features of glomus tumors are not characteristic, and the supplementation of clinical impressions with radiographic studies is uncommon . Glomus tumors typically occur in the skin of extremities but rarely in visceral organs. Glomus tumors in visceral organs are discovered incidentally or due to vague symptoms . Most glomus tumors are benign, but some with malignant potential have been reported. Herein, we report a case of glomus tumor with atypical features arising in the liver.
Glomus tumors usually occur in the skin of extremities and are rarely present in visceral organs, such as the gastrointestinal tract , mediastinum , bladder , kidney , or corpus cavernosum . Glomus tumors arising in the liver are extremely rare. To our knowledge, only six cases have been reported in the English literature, including the case presented herein [7–12].
The liver is the main target organ of metastasis. However, inspection of the present case prior to operation revealed no tumors in organs other than the liver, suggesting the tumor was not a metastatic lesion, but rather a primary tumor. It is necessary to distinguish glomus tumors from other tumor types, such as hemangioendotheliomas, gastrointestinal stromal tumors (GIST), paragangliomas, PEComas, and neuroendocrine tumors (NET). The lack of CD34 and ERG immunopositivity in conjunction with the histological appearance ruled out hemangioendothelioma. GIST and paraganglioma appeared to be ruled out because the tumor was CD117-, DOG-1-, S100-, and chromogranin A-negative. Concomitant positivity for synaptophysin and lack of melanosome positivity ruled out PEComa. NET is typically synaptophysin-, chromogranin A-, CD56-, and cytokeratin-positive. The present case was focally positive for synaptophysin, but negative for chromogranin A, CD56, CAM5.2, cytokeratin AE1/AE3, cytokeratin 7, and cytokeratin 19. The lesion was unlikely a hepatocellular carcinoma or hepatoblastoma, since both AFP and HepPar-1 were negative. Taken together, the findings suggest that the current tumor was a glomus tumor.
Glomus tumors are usually benign, but unusual histological features, including an infiltrative growth pattern, mitotic activity, and nuclear pleomorphism, have been reported in several cases. Folpe et al. analyzed 52 cases of glomus tumors with atypical histological features and defined a ‘malignant glomus tumor’ as that fulfilling at least one of the following criteria: (i) deep location and a size of more than 2 cm, (ii) atypical mitotic figures, or (iii) moderate-to-high nuclear grade and mitotic activity (more than 5 mitotic figures per 50 HPFs) . They defined the criteria based on the fact that metastatic lesion was observed in 38 % of tumors fulfilling the criteria, while metastasis was not seen in tumors not classified as ‘malignant glomus tumors’ . The problem with these criteria is that all glomus tumors arising in the liver meet the first criteria, since they are located in a deep space regardless of histological grade. Moreover, the glomus tumors reported in the liver to date are much larger than ordinary cutaneous glomus tumors (usually less than 1 cm). Kihara et al. stated that glomus tumors arising in visceral organs may be diagnosed belatedly because they have less intense symptoms and are less palpable . Folpe et al. analyzed only three cases of visceral organ tumors (two in the lungs and one in the stomach), but did not analyze those without histological atypia . Therefore, in agreement with Kihara et al. , we believe that liver glomus tumors cannot be classified as malignant on the basis of their location and size alone, and that histological evaluation described in the other two criteria (ii) and (iii) should be of value. None of the five hepatic glomus tumor cases reported thus far have displayed histological abnormalities [7–12]; this is the first case arising in the liver with histological atypical features. In the atypical-looking lesion, mitotic figures were frequently seen (35/50 HPFs), but nuclear atypia was not higher than a typical malignant glomus tumor . Atypical mitotic figures were not evident in the present case. Taken together, while the present case showed an invasive growth pattern and high mitotic figures, the tumor cells did not entirely meet the second the third (ii and iii) histological criteria listed above, and we therefore concluded that the current tumor was not a malignant glomus tumor.
One of the most interesting features of the present case was that the tumor cells were focally positive for synaptophysin. In general, glomus tumors in peripheral soft tissues are synaptophysin-negative, but reports of glomus tumors focally positive for synaptophysin have been documented [5, 14]. Interestingly, glomus tumors positive for synaptophysin occur not in peripheral soft tissues, but in visceral organs . More importantly, most of the reported glomus tumors positive for synaptophysin have atypical histological features. Song et al. reported a case of a malignant glomus tumor in the stomach that showed focal positivity for synaptophysin with prominent nuclear atypia and a fulminant course with multiorgan metastases . Zhang et al. also reported a malignant glomus tumor of the esophagus with mediastinal lymph node metastases that tested positive for synaptophysin and exhibited increased high mitotic activity . Moreover, other studies have reported cases of glomus tumors with atypical histological features and synaptophysin positivity in the kidney [5, 16], esophagus  and bronchus . Although there is one report of a case of glomus tumor without atypia that stained positive for synaptophysin , most cases of glomus tumors positive for synaptophysin exhibit either histological atypia or clinically malignant behavior, such as metastasis. These previous reports and the present case suggest that synaptophysin positivity may correlate with atypical histological features in glomus tumors arising in visceral organs.
In conclusion, we report an extremely rare case of a glomus tumor in the liver. Glomus tumors arising in visceral organs are very rare, as are those with atypical histological features, and little is known about the clinical course or prognosis of an uncommon glomus tumor. The types of glomus tumors in visceral organs with malignant courses, including metastasis, are also unknown. An accumulation of evidence regarding uncommon glomus tumors is indispensable to provide appropriate treatment and precisely estimate prognoses.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of written consent is available for review with the Editor-in-Chief of this journal.
- Mravic M, LaChaud G, Nguyen A, Scott MA, Dry SM, James AW. Clinical and histopathological diagnosis of glomus tumor: an institutional experience of 138 cases. Int J Surg Pathol. 2015;23:181–8.PubMed CentralPubMedView ArticleGoogle Scholar
- Miettinen M, Paal E, Lasota J, Sobin LH. Gastrointestinal glomus tumors: a clinicopathologic, immunohistochemical, and molecular genetic study of 32 cases. Am J Surg Pathol. 2002;26:301–11.PubMedView ArticleGoogle Scholar
- Gaertner EM, Steinberg DM, Huber M, Hayashi T, Tsuda N, Askin FB, et al. Pulmonary and mediastinal glomus tumors--report of five cases including a pulmonary glomangiosarcoma: a clinicopathologic study with literature review. Am J Surg Pathol. 2000;24:1105–14.PubMedView ArticleGoogle Scholar
- Tripodi SA, Rocca BJ, Mourmouras V, Barbanti G, Colecchia M, Ambrosio MR. Benign glomus tumor of the urinary bladder. Arch Pathol Lab Med. 2013;137:1005–8.PubMedView ArticleGoogle Scholar
- Gill J, Van Vliet C. Infiltrating glomus tumor of uncertain malignant potential arising in the kidney. Hum Pathol. 2010;41:145–9.PubMedView ArticleGoogle Scholar
- Masson-Lecomte A, Rocher L, Ferlicot S, Benoît G, Droupy S. High-flow priapism due to a malignant glomus tumor (glomangiosarcoma) of the corpus cavernosum. J Sex Med. 2011;8:3518–22.PubMedView ArticleGoogle Scholar
- Gassel HJ, Klein I, Timmermann W, Kenn W, Gassel AM, Thiede A. Presentation of an unusual benign liver tumor: primary hepatic glomangioma. Scand J Gastroenterol. 2002;37:1237–40.PubMedView ArticleGoogle Scholar
- Kenn W, Klein I, Gassel HJ, Gattenloehner S, Gassel AM, Hahn D. Primary glomangioma of the liver: imaging findings. Abdom Imaging. 2002;27:716–9.PubMedView ArticleGoogle Scholar
- Jaiswal VR, Champine JG, Sharma S, Molberg KH. Primary glomangioma of the liver: a case report and review of the literature. Arch Pathol Lab Med. 2004;128:e46–9.PubMedGoogle Scholar
- Geramizadeh B, Nikeghbalian S, Shamsaifar A, Kazemi K, Tavoosi H, Sefidbakht S, et al. Primary glomus tumor of the liver: a rare case report and review of the literature. Indian J Pathol Microbiol. 2011;54:584–7.PubMedView ArticleGoogle Scholar
- Amoueian S, Meibodi NT, Tavoosi H, Ekramifard VR, Attaranzadeh A, Montazer M. Primary glomus tumor of the liver. Arch Iran Med. 2011;14:294–5.PubMedGoogle Scholar
- Kihara A, Fukushima J, Horiuchi H. Glomus tumor of the liver presenting as a cystic lesion. Pathol Int. 2014;64:295–7.PubMedView ArticleGoogle Scholar
- Folpe AL, Fanburg-Smith JC, Miettinen M, Weiss SW. Atypical and malignant glomus tumors: analysis of 52 cases, with a proposal for the reclassification of glomus tumors. Am J Surg Pathol. 2001;25:1–12.PubMedView ArticleGoogle Scholar
- Song SE, Lee CH, Kim KA, Lee HJ, Park CM. Malignant glomus tumor of the stomach with multiorgan metastases: report of a case. Surg Today. 2010;40:662–7.PubMedView ArticleGoogle Scholar
- Zhang Y, Li H, Zhang WQ. Malignant glomus tumor of the esophagus with mediastinal lymph node metastases. Ann Thorac Surg. 2013;96:1464–6.PubMedView ArticleGoogle Scholar
- Lamba G, Rafiyath SM, Kaur H, Khan S, Singh P, Hamilton AM, et al. Malignant glomus tumor of kidney: the first reported case and review of literature. Hum Pathol. 2011;42:1200–3.PubMedView ArticleGoogle Scholar
- Bali GS, Hartman DJ, Haight JB, Gibson MK. A rare case of malignant glomus tumor of the esophagus. Case Rep Oncol Med. 2013;2013:287078.PubMed CentralPubMedGoogle Scholar
- Nakajima Y, Koizumi K, Haraguchi S, Kawamoto M, Kubokura H, Okada D, et al. Locally infiltrative glomus tumor of the bronchus: a case report. Ann Thorac Cardiovasc Surg. 2010;16:113–7.PubMedGoogle Scholar
- Jundi M, Lack EE, Brun EA, Esquivel J, Kumar D. Glomus tumor of the duodenum: a case report. Int J Surg Pathol. 2004;12:411–4.PubMedView ArticleGoogle Scholar
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.