Abstract

IntroductionCollecting duct carcinoma is a rare type of renal cell carcinoma. The primary is difficult to diagnose on imaging, and metastases are often present on initial presentation. Extensive multiorgan metastases can result in complex presentations that can be difficult to diagnose.Case presentationWe present two case reports of multiorgan metastases of collecting duct carcinoma that were autopsy confirmed. The first case was a 55-year-old man who presented with fever and abdominal pain. Abdominal computed tomography showed enlargement of the right kidney. Pyelonephritis was considered on the basis of laboratory test results and imaging findings. However, multiple cavitary lesions were found on routine chest radiography. These lesions were biopsied, resulting in a histological diagnosis of metastatic adenocarcinoma. A renal tumor was considered. Transitional cell carcinoma was suspected, which proved to be misdiagnosed and chemotherapy was given accordingly. However, this was not effective and the patient died after 2 months. Autopsy demonstrated the primary tumor to be collecting duct carcinoma, with metastases to lung, liver, spleen, bone marrow, right adrenal gland, and para-aortic lymph node. Computed tomography done while the patient was alive detected lung, liver, and para-aortic lymph node metastases. The second case was a 77-year-old man who presented with fever. Pyelonephritis was considered on the basis of the laboratory test results and imaging findings. Antibiotic therapy improved his symptoms and laboratory indicators of inflammation. One year later, he developed backache. Computed tomography revealed a progressively enlarging right renal lesion, multiple liver masses, enlargement of the para-aortic lymph nodes, and multiple osteoblastic and osteoclastic lesions. A renal tumor with multiple metastases was diagnosed. Chemotherapy was given without effect, and the patient died of cardiac failure 1 year later. Autopsy revealed a primary tumor of collecting duct carcinoma with metastases to the liver, right adrenal gland, right upper ureter, bone marrow, para-aortic and mediastinal lymph nodes, and bone.ConclusionWe present the radiological findings of lung, liver, lymph node, and bone metastases in two patients with collecting duct carcinoma.

Highlights

  • Collecting duct carcinoma is a rare type of renal cell carcinoma

  • Since patients with Collecting duct carcinoma (CDC) often have metastases at the time of presentation, and computed tomography (CT) findings of the primary tumor can be difficult to interpret, it is important to be familiar with the radiological features of metastatic CDC based on autopsy-confirmed cases

  • Laboratory tests and renal CT imaging were suggestive of pyelonephritis

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Summary

Introduction

Collecting duct carcinoma (CDC) is a rare type of renal cell carcinoma (RCC), accounting for 0.4% to 1.8% of all RCCs [1,2,3]. Since patients with CDC often have metastases at the time of presentation, and computed tomography (CT) findings of the primary tumor can be difficult to interpret, it is important to be familiar with the radiological features of metastatic CDC based on autopsy-confirmed cases. D. Computed tomography scan through the upper lung shows multiple cavitary lesions (arrows). The primary tumor was found to be a collecting duct carcinoma, and there were lung, liver, spleen, bone marrow, right adrenal gland, and paraaortic lymph node metastases. Based on CT findings (Figure 2A–C) and laboratory test results, pyelonephritis was initially suspected Antibiotic therapy improved his symptoms and laboratory indicators of inflammation. The primary tumor was found to be a collecting duct carcinoma, and liver, right adrenal gland, right upper ureter, bone marrow, para-aortic and mediastinal lymph node, and bone metastases were found

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