Metastatic Renal Cell Carcinoma of Mandible: A Case Report with Review of Literature

Article Information

Prabhanshu S*, Suchitra G, Dipak G, Nivedita K, Maya N

Department of Oral Pathology, Government Dental College & Hospital, Nagpur, India

*Corresponding Author: Prabhanshu Shrivastava, Department of Oral Pathology, Government Dental College & Hospital, Nagpur, India

Received: 09 December 2023; Accepted 18 December 2023; Published: 21 December 2023

Citation: Prabhanshu Shrivastava, Suchitra Gosavi, Dipak Ghatage, Nivedita Kaorey, Maya Nishad. Metastatic Renal Cell Carcinoma of Mandible: A Case Report with Review of Literature. Dental Research and Oral Health. 6 (2023): 95-98.

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Abstract

Metastatic lesions to the jaw bones are seldom found, but when observed pose a great diagnostic dilemma to the pathologists. In such cases, immunohistochemical markers and imaging modalities play a significant role in enabling the diagnosis. This case report discusses one such perplexing case of a metastasized renal cell carcinoma to the mandible with undiagnosed primary neoplasm. Discussed here is a case of a 66-year-old male who presented with a proliferative mass involving the left alveolobuccal complex.

Keywords

Metastasis, Renal Cell Carcinoma, Jaw bones

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Article Details

Introduction

Metastasis is a highly complex biological process that begins as the tumor cells detach from the primary tumor, spread into the distant tissues and/or organs, and invade through the lymphovascular structures followed by their survival in the circulation and subsequent proliferation in competent organs leading to colonization [1]. Metastatic tumors in the oral cavity are very rare, accounting for only 1%-3% of all malignant oral neoplasms [2]. The most common sites of primary malignancies are Breast, lung and kidney. In the orofacial region, the mandible is the most frequently affected site for metastases, particularly in the molar region. The peculiarity of these metastatic lesions is that they often show non aggressive clinical findings that frequently favours a reactive or benign lesions or odontogenic lesion [3]. The diagnosis of a metastatic lesion in the oral region is challenging, both to the clinician and to the pathologist. The clinician must recognize the possibility that a lesion may represent a metastasis, and the pathologist must determine the site of tumor origin [4]. Diagnosis of these metastatic tumours often require adjuvant investigations and advanced diagnostic procedures. This article discusses one such case with a perplexing clinical and histological picture which was diagnosed with the aid of immunohistochemical markers and advanced radiographic modalities.

Case Report

A 66 years old male patient reported to our OPD with chief complaint of pain and swelling in the lower left back region of the jaw since last 6 months. There was no history of bleeding or pus discharge from the site. He reported a bidi smoking habit 5 to 6 times a day for 20 years. Extra oral Examination revealed pain and swelling present on the left side of the mandible.

On palpation, a solitary, fixed and tender submandibular lymph node was noted. Intra orally, an ulceroproliferative growth was visible involving the Left alveolobuccal complex. Antero-posteriorly, the lesion extended from the mesial aspect of the mandibular left canine to the third molar on the same side. Vertical extension was from the crest of the alveolar bone and involving the buccal vestibule. The size of the lesion was approximately 4cm x 1cm. On inspection, the growth was pale pink in colour, had everted margins and indurated base. The patient had lost all his teeth on the affected side (Figure 1). Radiography revealed a large lytic lesion on left mandible presenting as an ill-defined bone resorption extending from symphyseal region till third molar and supero-inferiorly, from crest of alveolus till mandibular canal (Figure 2). CECT findings included a 25 × 15 × 10 mm sized heterogeneously enhancing lesion involving left lower alveolus causing expansion and lytic changes in bone. Medially the lesion was abutting floor of mouth and extension in the left sub lingual space. Laterally the lesion was involving lower GBS along its anterior aspect. Left mandibular canal appeared to be involved by the lesion. Based on the history and the clinical findings, a provisional diagnosis of squamous cell carcinoma of left alveolobuccal complex (ABC) was given and the patient was referred to the department of Oral Surgery for biopsy.

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Figure 1: Clinical image of the patient showing ulceroproliferative growth on left side of mandible.

Histopathology revealed multiple bits of tissue devoid of surface epithelium. Lesional tissue showed extensive proliferation of tumor cell population in the form of clear cells. These tumor cells were large and arranged in the form of small islands, cords and dissociated cells with hyperchromatic nuclei varying from round to pleomorphic in shape located central or eccentrically. Intervening connective tissue stroma was scanty and comprised of haphazardly arranged collagen fibers and chronic inflammatory cells (Figure 3). Part of the section showed numerous proliferative strands of tumor cells with abundant cytoplasm and large round to oval pleomorphic hyperchromatic nuclei in a stroma of hyalinized collagen fibers, fibroblasts and inflammatory cells. A differential diagnosis of Oral squamous cell carcinoma with clear cell variant, mucoepidermoid carcinoma, Clear cell odontogenic lesion and metastatic lesion was made. Immunohistochemical assay comprising of CK 14,19 and 20, EMA and vimentin were performed on the tissue sections to rule out tumours of salivary and odontogenic origin. Tumor cells stained positive for EMA and Vimentin (Figures 4 and 5) both of which are strong indicators of metastasis. The patient was further advised to undergo Chest X-ray (CXR) and Ultrasonography (USG)of the abdomen. CXR revealed no active pleuro-parenchymal lesion. USG abdomen reported well-defined round to oval heterogeneously isoechoic to hyperechoic lesion of size 3.4 X 2.8 cm in relation to upper pole of right kidney. Correlating the findings and the diagnostic results, we arrived at a final diagnosis of metastatic renal cell carcinoma. The patient provided the informed consent for publication of this case.

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Figure 2: Radiograph of the patient showing large lytic lesion on left mandible presenting as an ill-defined bone resorption

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Figure 3: H & E-stained section (10X) showing proliferation of tumor cell population in the form of clear cells

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Figure 4: Immunohistochemistry showing EMA positivity

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Figure 5: Immunohistochemistry showing Vimentin positivity

Discussion and Review of literature

Renal cell carcinoma (RCC) accounts for 3% of adult malignancies and 90% to 95% of kidney tumors [4]. The rate of metastasis in RCC is reported to be around 30% [5,6]. RCC has been known metastasize to distant organs, including bilateral adrenal glands, skin, pancreas and spleen, gastric or duodenal systems, skeleton, pancreas and bladder. However, reports of metastases to the head and neck region have been extremely rare [7]. The incidence of oral metastases and their origins may vary according to the study population. Boles R and Cerny J, reported the incidence of metastasis from RCC to head and neck to be 15% [8]. According to Hirshberg et al. the kidney is the third most common primary site for oral metastases [9]. As was seen in our case, jaw lesions were the first reported manifestation of an undiagnosed primary malignancy. The common clinical features of this oral metastatic disease include submucosal or jaw mass, jaw or oral pain, lip numbness, gingival swelling, or even an extensive bilobed mass. Bleeding, tooth mobility, trismus, paraesthesia, and paralysis may be accompanying findings in some cases. Radiography may reveal extensive lytic lesions of the jaw bones with ill defined, irregular margins. Further imaging modalities like USG abdomen and PET scan etc. facilitates the diagnosis of the underlying primary or further metastasized masses [10]. According to the literature review by Naoto Nishii et al, a distinct male predominance was observed with the male to female ratio being 3:1 with mean age of 61.4 years. The tongue was involved in renal metastases in most patients (39%) followed by mandible(19.1%). Out of the 153 cases reviewed, they found that 58 cases were diagnosed before the diagnosis of primary RCC and 93 after the primary malignancy was diagnosed [11]. Our patient was a 66 year old male with mandibular involvement wherein the oral lesion was the first clinical manifestation of the primary neoplasm. Clinically the lesion mimicked a squamous cell carcinoma.  Histopathology of clear cell renal cell carcinoma depicts significant vascularisation, cells with pleomorphic and hyperchromatic nuclei and cells with a clear cytoplasm [12,13]. As was observed in our case, if the primary neoplasia was undiagnosed immunohistochemical assay was mandatory to establish the diagnosis. The main markers in the panel include PAX8, presenting positivity in approximately 90% of cases, and CD10 with positivity in 98%. Another classic marker is AE1/AE2, positive in 88% of the cases. The reported case was negative for this marker, which can be explained by its poorly differentiated cells [14]. In addition to these markers, another that can be used is CK7, an important marker for epithelial tumours and with high expression in renal tumors [15]. Management primarily includes radiotherapy and chemotherapy- pazopanib, sunitinib and sorafenib. These drugs are angiogenic inhibitors which target VEGF receptors resulting in decreased tumour volume [16,17]. Surgical management is opted after the tumor size is reduced. Literature review of similar cases revealed the longest survival time to be 11 months and smaller survival time to be around six months [18,19].

Conclusion

Owing to their rarity, diagnosis of oral metastatic diseases is a challenge pathologists encounter. In these cases, stress lies upon the judicious and optimal utilisation of the advanced diagnostic techniques along with histopathology to arrive at an accurate diagnosis.

References

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