Unusual Renal and Colonic Mass: Description of a Rare Case
CC BY-NC-ND 4.0 · Indian J Med Paediatr Oncol 2019; 40(S 01): S154-S156
DOI: DOI: 10.4103/ijmpo.ijmpo_190_17
Abstract
Seminoma is a germ cell tumor which accounts for approximately 40% of all germ cell tumors. Testicular seminoma is usually localized to the testis, and in 25% of cases, lymph node metastasis is seen. However, rarely, it can metastasize to visceras. We report a rare case of metastatic seminoma in a 40-year-old male who presented with renal and intestinal mass 2 years after orchidectomy.
Publication History
Article published online:
24 May 2021
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Abstract
Seminoma is a germ cell tumor which accounts for approximately 40% of all germ cell tumors. Testicular seminoma is usually localized to the testis, and in 25% of cases, lymph node metastasis is seen. However, rarely, it can metastasize to visceras. We report a rare case of metastatic seminoma in a 40-year-old male who presented with renal and intestinal mass 2 years after orchidectomy.
Introduction
Visceral metastases of seminoma at presentation can be seen in <5 href="https://www.thieme-connect.com/products/ejournals/html/10.4103/ijmpo.ijmpo_190_17#JR_1" xss=removed>1] We report a rare case of metastatic seminoma in a 40-year-old male who presented with renal and intestinal mass 2 years after orchidectomy for seminoma.
Case Report
A 40-year-male was admitted with chief complaints of swelling in the left flank and abdominal discomfort for 2 years. The swelling was gradually increasing in size and was not associated with fever, hematuria, or constipation. The patient was a chronic smoker. Hematological and biochemical investigations were within normal limits. X-ray chest was normal. Ultrasonography abdomen suggested a left renal mass with tumor emboli in the left renal vein and inferior vena cava lumen. Computed tomography abdomen was done and showed left renal mass at the lower pole with complete encasement of ipsilateral ureter, renal artery, and vein. Tumor was extending medially up to the aorta with mild paravertebral extension at L2 into the para-aortic lymph nodes and infiltration of the psoas muscle and colon [Figure 1]. Fine needle aspiration cytology was done from outside which showed single and small groups of atypical cells with eccentric hyperchromatic nuclei and focally appreciable vacuolated cytoplasm against a hemorrhagic background. Cytological diagnosis was malignant tumor with a possibility of clear cell renal carcinoma.
The patient underwent nephrectomy, adherent segmental colectomy along with left ureteric and para-aortic lymph node excision.
Histopathological Examination
The kidney measured 8.5 cm × 5 cm × 3 cm with adherent 9.5 cm of the colon. External surface of the kidney appeared gray-white and encapsulated except for the area where the segment of the intestine was adherent. Serial slicing revealed a poorly circumscribed firm white nodular lesion toward the lateral surface. Pelvicalyceal system was dilated with a clot in the hilar area. Two para-aortic lymph nodes were also identified measuring 3 cm × 2 cm × 1 cm and 2 cm × 1 cm × 1 cm. The tumor was infiltrating into the adherent large intestine.
On microscopy, multiple sections from the renal mass showed prominent fibrohistiocytic proliferation [Figure 2a], confluent epithelioid cell granulomas, lymphocytic infiltrate, and giant cells. Intervening areas and the pelvis were infiltrated by single as well as nests of tumor cells. The cells were showed moderate nuclear pleomorphism, vesicular chromatin, prominent nucleoli, and scant-to-moderate amount of clear cytoplasm [Figure 2b]. Large areas of necrosis were also noted. The tumor was infiltrating the renal capsule. Ten para-aortic lymph nodes were identified, out of which five showed tumor deposits; however, the ureter was free of tumor. Multiple sections from the large intestine showed infiltration by the tumor [Figure 2c].