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CASE REPORT |
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| Year : 2016 | Volume
: 20
| Issue : 2 | Page : 331 |
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Primary osteoclast-like giant cell tumor of parotid gland: A rare extraskeletal presentation with diagnostic challenges
Ritika Singh, Sufian Zaheer, Ashish K Mandal
Department of Pathology, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India
| Date of Submission | 06-Jun-2015 |
| Date of Acceptance | 06-Jun-2016 |
| Date of Web Publication | 11-Jul-2016 |
Correspondence Address:
Ritika Singh
F-6, Police Station, Chanakyapuri, New Delhi - 110 021
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0973-029X.185903
 Abstract | | |
Primary osteoclast-like giant cell tumor (OC-GCT) has been rarely described in extraskeletal sites. The diagnosis primarily hinges on the detection of giant cells. However, these giant cells are also seen in many giant cell lesions, thus creating diagnostic confusion and dilemma. Here, we describe a rare case of a 24-year-old male with primary extraskeletal, OC-GCT presenting as a swelling in the right parotid region and highlight its cytological, histological and immunohistochemical characteristics with diagnostic challenges.
Keywords: Extraskeletal GCT, osteoclast-like giant cell, parotid region
How to cite this article:
Singh R, Zaheer S, Mandal AK. Primary osteoclast-like giant cell tumor of parotid gland: A rare extraskeletal presentation with diagnostic challenges. J Oral Maxillofac Pathol 2016;20:331 |
How to cite this URL:
Singh R, Zaheer S, Mandal AK. Primary osteoclast-like giant cell tumor of parotid gland: A rare extraskeletal presentation with diagnostic challenges. J Oral Maxillofac Pathol [serial online] 2016 [cited 2021 Feb 27];20:331. Available from: https://www.jomfp.in/text.asp?2016/20/2/331/185903 |
| Introduction | |  |
Primary osteoclast-like giant cell tumor (OC-GCT) has been reported in skeletal and extraskeletal sites such as pancreas,[1] urinary bladder,[2] thyroid [3] and liver.[4] It is a rare tumor of the salivary gland with very few histopathologically confirmed cases, which have been reported in world literature.
Twenty-four cases have been described previously in the salivary gland, of which parotid gland involvement was reported in twenty cases,[5],[6],[7],[8],[9],[10],[11],[12],[13],[14],[15],[16],[17],[18],[19],[20] followed by submandibular gland involvement in three cases [20],[21],[22] and the minor salivary gland in one case.[22] It presents as a rapidly enlarging mass, which may or may not be painful.
| Case Report | | |
A 24-year-old male presented with a swelling in the right parotid region for the past 2 years. The swelling had increased in size over the last 6 months. Physical examination revealed a firm, nontender mass measuring 5 cm × 3 cm.
Radiological findings
Computed tomography scan of the head and neck showed a heterogeneous solid mass arising from the superficial lobe of the right parotid region extending superiorly in the subcutaneous plane of the right temporal region with no bony fixation or erosion, suggesting primary involvement of the parotid gland [Figure 1]a. | Figure 1: (a) Computed tomography scan of head and neck showing a solid mass arising from the superficial lobe of the parotid gland. No bony fixation or erosion noticed. (b) Numerous regularly distributed osteoclast-like giant cells with oval-to-spindle mononuclear cells (Giemsa stain, ×200). (c) Gross photograph showing an ill-defined, gray-tan tumor with areas of hemorrhage and congestion. (d) Biphasic tumor with osteoclast-like giant cells and mononuclear cells which show nuclear irregularity and hyperchromasia along with foci of osteoid formation (H&E stain, ×400). Inset shows tumor with residual salivary gland tissue (H&E stain, x100)
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Cytological findings
Aspiration from the swelling yielded an adequate sample. The Giemsa-stained smears were prepared, which on microscopy were cellular, revealing numerous regularly distributed osteoclast-like giant cells along with mononuclear cells present in clusters and scattered individually. Osteoclast-like giant cells showed multiple nuclei ranging from 5 to 50. The mononuclear cells were of variable shapes and sizes and were round, oval and spindled. Some of these cells had high nuclear-cytoplasmic ratio [Figure 1]b. A cytological diagnosis of a tumor/lesion rich in giant cells was suggested.
Histopathological findings
The patient underwent right parotidectomy. Grossly, the specimen measured 5 cm × 3.5 cm × 3 cm. Its cut surface showed ill-defined, gray-tan tumor measuring 5 cm × 3 cm × 2.5 cm with focal areas of hemorrhage and congestion [Figure 1]c. The surgical margins were not involved by the tumor.
Microscopic examination revealed a cellular, poorly circumscribed biphasic tumor consisting of numerous regularly distributed osteoclast-like giant cells along with mononuclear cells. The osteoclast-like giant cells had sharp cellular borders with abundant acidophilic cytoplasm and multiple nuclei varying in number from 5 to 50. Their nuclei were round to oval and vesicular with prominent nucleoli. The giant cell nuclei did not show any pleomorphism or atypia.
The mononuclear cells had moderate-to-scant amount of acidophilic cytoplasm with oval-to-spindle-shaped nuclei showing nuclear irregularity, most of the nuclei had vesicular chromatin whereas few mononuclear cell nuclei were hyperchromatic [Figure 1]d. Mitotic activity was low with a count of 0–2 mitosis/10 high-power fields with no atypical mitosis. Stromal hemorrhage was present along with focal areas showing osteoid formation.
Immunohistochemical finding
On immunohistochemical analysis, the osteoclast-like giant cells showed diffuse cytoplasmic positivity for vimentin and CD68. They were negative for cytokeratin (CK), S100 and smooth muscle actin (SMA). Mononuclear cells showed cytoplasmic positivity for vimentin and focal positivity for CD68. The mononuclear cells with hyperchromatic irregular nuclei which were focally present showed positivity for CK. S100 and SMA were negative [Figure 2]a,[Figure 2]b,[Figure 2]c. With radiological, cytological, histological and immunohistochemical findings in consideration, a final diagnosis of OC-GCT of the parotid gland was rendered. | Figure 2: (a) Vimentin positivity in osteoclast-like giant cells and mononuclear cells (IHC stain, ×200). (b) CD68 positivity seen in osteoclast-like giant cells and some mononuclear cells (IHC stain, ×200). (c) Focal cytokeratin positivity in mononuclear cells (IHC stain, ×400)
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| Discussion | | |
Primary OC-GCT of the salivary gland was first described in 1984 by Eusebi et al. in the parotid gland.[5]
Since then, 24 cases have been described in the salivary gland, of which parotid gland involvement was reported in twenty cases,[5],[6],[7],[8],[9],[10],[11],[12],[13],[14],[15],[16],[17],[18],[19],[20] followed by submandibular gland involvement in three cases [20],[21],[22] and the minor salivary gland in one case.[2] The tumor is five times more common in males than in females and generally presents between 28 and 92 years of age.[5],[6],[7],[8],[9],[10],[11],[12],[13],[14],[15],[16],[17],[18],[19],[20],[21],[22]
In the previously reported cases, the association of primary OC-GCT of the salivary gland with coexisting benign neoplasm (pleomorphic adenoma in two cases)[12],[20] and malignant neoplasms (carcinoma in 13 cases)[5],[6],[7],[8],[9],[11],[13],[14],[15],[18],[19],[21],[22] has been reported. The tumor is also known to exist as a “pure form” without any associated neoplasm (nine cases).[5],[7],[10],[16],[17],[19] The review of previous cases is presented in [Table 1].[5],[6],[7],[8],[9],[10],[11],[12],[13],[14],[15],[16],[17],[18],[19],[20],[21],[22] | Table 1: Summary of the previously described osteoclast-like giant cell tumor of the salivary gland cases
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In the present case, the radiological evaluation suggested the presence of a tumor arising from the parotid. No soft tissue or bony involvement was seen ruling out any primary tumor that may arise from these sites, which may involve the salivary gland.
Cytological findings in the present case revealed a bimodal cell population with benign-appearing osteoclast-like giant cells and pleomorphic population of mononuclear cells. Histopathology confirmed the presence of a pure form of OC-GCT of parotid gland with a biphasic cell population consisting of benign-appearing osteoclast-like giant cells, the presence of which raised a possibility of an underlying OC-GCT of the bone and mononuclear cells. The OC-GCT of bone has numerous regularly distributed osteoclast-like giant cells in a mononuclear cell population. However, histopathology of these mononuclear cells is unlike that of OC-GCT of the salivary gland, in which nuclear pleomorphism and hyperchromasia are present, and it is an important finding to differentiate the two.[5],[9],[11],[15],[20]
A possibility of giant cell granuloma was also considered as needle aspiration showed many osteoclast-like giant cells with mononuclear cells with few atypical cells, however unlike OC-GCT of the salivary gland, giant cell granuloma is smaller in size with fewer and smaller nuclei in the osteoclast-like giant cells.[8]
A possibility of giant cell carcinoma or undifferentiated carcinoma with anaplastic giant cells needs to be excluded which histologically shows an anaplastic tumor with bizzare highly pleomorphic giant cells whereas in OC-GCT of the salivary gland, has a bland appearance.
Possibility of soft tissue tumors with giant cells was also ruled out histopathologically along with primary epithelial tumor of the salivary gland.
Immunophenotypically, in the present case, both giant cells and mononuclear cells expressed CD68 and vimentin. Focal cytoplasmic expression of CK in mononuclear cells was seen, which has been noted in the previously reported cases.[6],[7],[11],[17],[18] This expression of epithelial marker is not found in the mononuclear cells of OC-GCT of the bone and is seen rarely in OC-GCT of soft tissue. In the present case, clinical and radiological details and the presence of the tumor in the substance of parotid gland excluded the possibility of OC-GCT of bone.
GCT-like neoplasm in other parenchymal organs has been described, but it has been classified as “undifferentiated carcinoma with osteoclast-like giant cells.”[11] OC-GCT of the salivary gland is not included in the above category, and compared to undifferentiated carcinoma of the salivary gland, OC-GCT of the salivary gland shows male predominance, lesser degree of cellular atypia and a favorable 5-year survival rate.[15]
Some authors believe that OC-GCT of the salivary gland is a carcinoma and prefer the terminology of “osteoclast-type giant cell carcinoma” instead of “undifferentiated carcinoma with osteoclast-like giant cells”[11],[13] to avoid confusion with a high-grade carcinoma because of the following reasons:
- In many of the previously reported cases, there is an association with a carcinomatous component which many a times may be very small, necessitating a diligent search
- Expression of both epithelial and histiocytic markers by the mononuclear cells
- The microsatellite pattern of the giant cell tumor component is more akin to carcinomas reported by some studies.[11]
However, in spite of all the efforts, the origin of this tumor still remains controversial. Even though epithelial marker expression in mononuclear cells has been reported, in some of the cases,[5],[15],[16],[20] no epithelial marker expression was found; adding further to the existing diagnostic dilemma.
Even electron microscopic studies have suggested histiocytic [5] origin in some cases, but some have suggested an epithelial origin of the mononuclear cell.[6]
Despite the controversy surrounding the tumor origin, treatment involves a complete excision of the tumor with adequate surgical margin which warrants a long disease-free survival even in cases with co-existent carcinomatous foci.[16] Postoperative radiotherapy is also advised under conditions where negative surgical margins may only be achieved with increased morbidity or if surgery has been contraindicated.[16]
| Conclusion | | |
To conclude, identification of OC-GCT of the salivary gland on histopathology or cytology should warrant extensive sampling to rule out any associated neoplasm, especially carcinomatous foci. In addition, a detailed evaluation is needed to establish the tumor origin and histogenesis.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2]
[Table 1]
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