Primary epithelioid angiosarcoma originating from the mandibular gingiva: a case report of an extremely rare oral lesion

Abstract

Background

Angiosarcomas account for only 2% of all soft tissue sarcomas [1–3]. More than 50% of all cases occur in the head and neck region, with the scalp and forehead being the most common sites [4]. However, primary angiosarcomas in the oral cavity represent only 1% of all angiosarcomas [5]. Angiosarcoma generally exhibits an aggressive clinical course and an unfavorable prognosis, even in cases where surgical removal of the tumor is possible. Affected patients usually do not benefit from chemoradiotherapy [6]. Approximately 50% patients die within 15 months after diagnosis, and only 12% survive for 5 years or longer [7]. Generally, well-differentiated tumors have been associated with better survival rates. Tumor-related death is usually due to uncontrolled local progression and/or distant metastases to the lungs, liver, and bone [1, 8]. Early detection and treatment are essential for controlling this highly malignant soft tissue tumor.

Epithelioid vascular neoplasm is a unique tumor characterized by proliferating “epithelioid” or “histiocytoid” endothelial cells showing a sheet-like growth pattern with vascular differentiation [9–11]. Epithelioid angiosarcoma (EA) is a rare variant characterized by the proliferation of atypical, large, polygonal, epithelioid endothelial cells [12].

Until now, only four cases of primary EA in the jaw region have been reported, with three lesions originating in the maxilla and one in the mandible [2, 11, 13, 14]. A few cases of metastatic EA have also been reported [15–17]. To our knowledge, there is no reported case of EA involving the mandibular gingiva except pathological review of EA by Nagata et al. [2]. Here, we report a case involving an elderly man with a primary EA that originated from the mandibular gingiva and resembled a dentigerous cyst on radiographs.

Case presentation

A 66-year-old Japanese man visited a private dental office with a chief complaint of gingival swelling around right mandibular third molar. Considering the diagnosis of pericoronitis, the dentist performed incisional drainage and prescribed antibiotics and analgesics; however, the swelling reappeared with mild gingival bleeding 20 days after his first visit to the dental office. The dentist repeated incisional drainage and prescribed antibiotics, both of which were ineffective. The gingival swelling and oozing persisted; therefore, curettage of the swollen gingiva was performed. The dentist further referred the patient to our university hospital for extraction of the third molar, and he presented at our department 18 days after curettage of gingiva.

The patient’s medical history included controlled hypertension and cholecystectomy for gallstones. Hematological and biochemical examinations did not reveal any abnormalities. His facial profile was symmetrical, and the submandibular lymph nodes showed no tenderness or swelling on ultrasound. Intraoral examination revealed a dark purple gingival swelling with easy bleeding around the crown of right mandibular third molar (Fig. 1a). The mass measured 1.5 × 1.5 cm and covered the tooth crown. A panoramic radiograph showed that right mandibular third molar was mesially impacted, with bone resorption around the crown (Fig. 2a). Considering the clinical course of the lesion, pericoronitis was ruled out and incisional biopsy was performed under local anesthesia (Fig. 1b). The specimen was submitted for microscopic examination. Histopathological examination showed an angiosarcoma. At the time of biopsy, cone beam computed tomography (CBCT) showed mild bone consolidation (Fig. 2b) while T2-weighted magnetic resonance imaging showed high signal intensity (Fig. 2c) around the involved tooth. The region to be imaged with gadolinium was recognized; this suggested inflammation after biopsy and/or malignancy. None of the imaging studies, including fluorodeoxyglucose (FDG) positron emission tomography-computed tomography, showed significant swelling of and accumulation of FDG in the cervical lymph nodes (data not shown).

Surgical treatment with vascularized free flap reconstruction was planned. However, 4 weeks after the biopsy, the lesion exhibited aggressive proliferation perhaps because of traumatic irritation by the antagonist teeth. This led to uncontrolled bleeding and difficulty in closing the mouth (Fig. 1c). The treatment plan was changed and emergent mandibular resection without surgical reconstruction was performed. An incision extending from the lower lip to the sub-mandible was made. A safety margin of ≥ 10 mm was set, a periosteal flap was raised, and the mandibular body was identified. Right mandibular first premolar was extracted to establish the anterior border of the resection. The sublingual gland was preserved and the tumor was resected en bloc with the oral floor membrane and buccal mucosa (Fig. 2d).

The patient’s postoperative course was uneventful except for a delayed wound healing of the oral mucosa. Nevertheless, because the tumor had exhibited an aggressive preoperative course, he received adjuvant chemotherapy 2 months after the surgery [18]. Radiation therapy was deemed unnecessary. Paclitaxel (80 mg/m²) was administered once a week for 3 weeks, followed by a 1-week rest period. This cycle was repeated for 1 year. The patient showed no signs of recurrence during the 1-year follow-up period.

Histopathologically, the tumor was composed of solid sheets with incomplete alveolar structures (Fig. 3a) and no clear vasoformation. Large, densely packed cells with spindle, oval, polygonal, or bizarre shapes could be observed. The cells exhibited abundant amphophilic cytoplasm, large vesicular nuclei, and a few prominent nucleoli. Mitotic figures were scattered throughout the tumor. Keratinization and intercellular bridges were not obvious. Immunohistochemical analysis revealed positivity for vimentin (Fig. 3b), CD31 (Fig. 3c), and factor VIII (Fig. 3d) and negativity for epithelial, neural, muscular, and other markers. The Ki67 index was > 40% (Table 1). All of above the features are diagnostic for EA.

Discussion and conclusions

EA is a rare endothelial cell malignancy. Epithelioid endothelial cell tumors include epithelioid hemangioma, epithelioid hemangioendothelioma (EHE), and EA [14]. Epithelioid hemangioma is a benign tumor while EHE is a low-grade malignancy. EA is the least common type, and it is a high-grade malignancy characterized by atypical, multilayered, or solid endothelial proliferation and a vasoformative architecture on microscopic findings. EA displays a greater degree of nuclear pleomorphism and mitotic activity than does EHE and frequently shows areas of necrosis [19, 20]. Proposed criteria for distinguishing EA from other histopathological entities include a multilayered endothelium and an infiltrative growth pattern. Poorly differentiated angiosarcomas are best distinguished from other spindle cell sarcomas or carcinomas by immunohistochemistry. In particular, CD31 is the most sensitive endothelial marker [14, 19–21].

Angiosarcoma may be difficult to diagnose because of its various clinical and pathological characteristics [2]. Differential diagnoses include hemangioma, pyogenic granuloma, Kaposi’s sarcoma, melanoma, and metastatic disease [13, 14, 19, 20]. In the present case, primary EA of the mandibular gingiva was initially diagnosed as pericoronitis involving the mandibular third molar. In addition, CBCT suggested a hyperplastic dental follicle or a dentigerous cyst, and there were no signs of malignancy in imaging studies. Generally, radiographic findings for angiosarcoma may include osteolytic changes with a mild periosteal reaction [22]. Reviewing previous reports, it seems that the swelling of the gingiva accompanied by bone destruction with rapid growth of tumor (Table 2) [2, 11, 13–17]. In these cases, although the lesion may have originated from bone tissue, relatively well-defined margins may simulate a benign osteolytic lesion such as a cyst or an odontogenic tumor. There was a possibility that this tumor originated from bone tissue, however, the only clinical signs in the present case were gingival swelling and oozing, which is justified considering the origin of the tumor before osteolytic changes. The tumor enlarged rapidly after biopsy. Traumatic irritation by the antagonist teeth might accelerate the tumor growth, however, there is a possibility that this finding was due to the natural course of this rare aggressive tumor. Definitive diagnosis of angiosarcoma is challenging because of its rarity and clinical, radiographic, and histopathological resemblance to other diseases. Immunohistochemistry is generally required to identify this tumor, particularly the epithelioid and spindle cell types [2].

In immunohistochemistry, positive staining for factor VIII, CD34, and CD31, which are endothelial markers, indicates that the tumor has endothelial characteristics. The lesion in our patient showed positivity for factor VIII, CD31, and vimentin. In particular, CD31, a membrane glycoprotein that is important for endothelial cell-cell interactions and vascular adhesion of leukocytes, is considered the best marker for the endothelial phenotype, especially the poorly differentiated variant [23]. Our patient also exhibited a very high Ki67 index (> 40%).

Most authors believe that surgery in combination with radiotherapy and/or chemotherapy offers the best chance of survival [14]. Angiosarcomas exhibit a strong tendency for local recurrence and metastasis [13]. These characteristics reflect the highly aggressive nature of this tumor. Our patient received postoperative adjuvant chemotherapy because of the aggressive preoperative course of the lesion. The prognosis of angiosarcoma is unfavorable, although the tumor size and site and the histopathological grade may influence survival [24]. In particular, a poor prognosis is associated with advanced age, larger tumors, the tumor location, and a Ki67 index of > 10% [25]. Radical surgery should be performed as soon as possible for improvement of the prognosis [2].

Conclusions

We reported a rare case of a primary EA originating from the mandibular gingiva in an elderly man. To our knowledge, this is the first report of EA in the mandible, and the findings highlight the importance of early diagnosis and adequate surgical resection, which should be performed as soon as possible.

Acknowledgements

The authors would like to thank Editage (www.editage.jp) for English language editing.

Abbreviations

EA

Epithelioid angiosarcoma

EHE

Epithelioid hemangioendothelioma

CBCT

Cone beam computed tomography

FDG

Fluorodeoxyglucose

Authors’ contributions

YK, YO, OM, HY, and IM reviewed the literature. YO, KS, DS, and KK performed the operation and analyzed and interpreted the patient’s data. YT performed the histopathological analyses. YK, YO, KS, DS, KK, OM, IM, and HY were clinically responsible for the patient’s care. All authors have read and approved the final manuscript.

Funding

This study did not receive any funding.

Availability of data and materials

The datasets used during the current study are available from the corresponding author on reasonable request.

Ethics approval and consent to participate

This study was exempted from ethics approval by the Ethics Committee of Iwate Medical University, School of Dentistry, Morioka, Japan.

Consent for publication

The patient provided written informed consent for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of the journal.

Competing interests

The authors declare that they have no competing interests.

Footnotes

Contributor Information

Yuko Komatsu, Email: yuko@iwate-med.ac.jp.

Ikuya Miyamoto, Email: ikuyam@iwate-med.ac.jp.

Yu Ohashi, Email: yohashi@iwate-med.ac.jp.

Katsunori Katagiri, Email: kats460129@yahoo.co.jp.

Daisuke Saito, Email: daisaito@iwate-med.ac.jp.

Mizuki Obara, Email: mizuki@iwate-med.ac.jp.

Yasunori Takeda, Email: ytakeda@iwate-med.ac.jp.

Kiyoto Shiga, Email: kshiga@iwate-med.ac.jp.

Hiroyuki Yamada, Email: yamadah@iwate-med.ac.jp.

References

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