Concurrent occurrence of renal cell carcinoma with rhabdoid features in a married couple: a case report

Background Renal cell carcinoma (RCC) with rhabdoid features is a rare histology and exhibits clinically aggressive behavior. We report a case of a married couple in whom RCC with rhabdoid features concurrently occurred. The rarity of this event suggests that environmental factors may contribute to the etiology of RCC with rhabdoid features. Case presentation A 76-year-old Japanese woman was diagnosed with a hypervascular mass in the right kidney and tumor thrombus extending into the right atrium by enhanced computed tomography (CT). She underwent radical nephrectomy and tumor thrombectomy following systemic therapy with the tyrosine kinase inhibitor sunitinib. The histological evaluation denoted clear cell RCC with rhabdoid features. The patient died of cancer 12 months postoperatively. A 76-year-old man, her husband, presented with gross hematuria 2 weeks after his wife had undergone surgery. He had a long history of asbestos exposure. An abdominal CT scan revealed a hypervascular mass in the right kidney and tumor thrombus extending into the inferior vena cava. He also underwent radical nephrectomy and tumor thrombectomy. The histological evaluation also showed clear cell RCC with rhabdoid features. Bone metastasis occurred 12 months postoperatively, but he died of an unrelated cause 18 months after surgery. Conclusion Concurrent occurrence of RCC with rhabdoid features may not to be coincidental. Although further studies are warranted, asbestos exposure may contribute to the etiology of clear cell RCC with rhabdoid features.


Background
In large consecutive series of patients with malignant renal tumors, approximately 3-5% of RCCs showed rhabdoid features [1][2][3][4]. Generally, RCCs with rhabdoid features are highly aggressive malignant tumors and are associated with a poor prognosis. Compared with nonrhabdoid RCCs, these tumors are more likely to present at higher grades, twice as likely to undergo extrarenal invasion, and more likely to metastasize [1]. Microscopically, rhabdoid cells are usually associated with a clear cell RCC component and sometimes linked to sarcomatoid changes [1,3,4]. Rhabdoid cells have large, eccentric nuclei and abundant cytoplasm containing eosinophilic inclusions that are strongly positive for vimentin. In this article, we present very rare cases of a married couple in whom clear cell RCC with rhabdoid features and sarcomatoid change concurrently occurred. Coincidental concurrent occurrence is unlikely, suggesting that environment may be an etiologic factor for such a tumor.

Case 1
A 75-year-old womanwas referred to our hospital in May 2009 because enhanced computed tomography (CT) had confirmed the presence of a 70 mm mass on the upper pole of her right kidney and tumor thrombus extending into the right atrium ( Figure 1a). Based on a chest CT scan, the patient was initially suspected of having lung carcinoma. Because additional diagnostics were needed to exclude lung carcinoma, systemic therapy was initiated with the tyrosine kinase inhibitor sunitinib. After 4 cycles of sunitinib therapy, tumor regression was observed and the lung tumor had not changed. In December 2009, she underwent right radical nephrectomy and tumor thrombectomy.
Postoperatively, the patient developed acute renal failure secondary to circulatory insufficiency, and she received hemodialysis for about a month. The pathological diagnosis of the tumor was clear cell carcinoma with rhabdoid features and sarcomatoid change (assessed in the post-sunitinib therapeutic state; Figure 2a

Background factors of cases 1 and 2
The man and women whose medical cases are described above have been married for >40 years. Neither of them had any remarkable medical history. Their daughter had died of pancreatic cancer, but parents, siblings, and their son had no history of malignancy. The husband was a shipyard worker and had been exposed to asbestos for >30 years. Additionally, the chest CT scan revealed that he had slight light pleural thickening. Although his wife was not employed, she routinely came into contact with his hair and clothing and could have been exposed to asbestos. The couple did not report any other unusual occupational exposures, such as organic solvents or cadmium. The couple had lived in Hokuto city for 50 years, and there was no report of significant increases in the incidence of RCC within that area.

Conclusions
Familial RCC is well known, including von Hippel-Lindau disease and Birt-Hogg-Dube syndrome. However, spousal RCC has not been reported previously.
The synchronous occurrence of RCC with rhabdoid features in this married couple is unlikely to have been purely coincidental. Exposure to asbestos has generally been associated with malignant mesothelioma in humans. It has long been recognized that some patients with mesothelioma result from household exposure to asbestos that is brought home in workers' hair, clothing, and personal effects [5]. In a study of the wives of asbestos-exposed workers, Miller reported a mean latency of 45.4 years between the year of first exposure and the onset of symptoms of malignant mesothelioma [5]. RCC is also considered an occupationally associated tumor, but the existence of an association between RCC and asbestos exposure is currently controversial [6][7][8][9][10]. A recent genetics study of RCC found that rhabdoid features and high grade were associated with loss of BAP1, a nuclear deubiquitinase that regulates cell proliferation [11]. BAP1 copies are also lost in mesothelioma [12,13]. Furthermore, Carbone et al. have speculated that BAP1 may help prevent environmental carcinogenesis caused by asbestos [14]. Additionally, a few patients with concomitant RCC and malignant mesothelioma have been reported in Japan, although the reports of these cases have not indicated whether the RCC histologies were clear cell carcinoma with rhabdoid features [15]. In these cases, the development of RCC also occurred several decades after asbestos exposure. However, pathogenesis was not discussed in the associated case reports. Jiang et al. identified several novel characteristics of asbestos fibers in asbestos-induced oxidative DNA damage. By studying intraperitoneal administration of asbestos fibers in rats, Jiang et al. also found that the kidney was oxidatively stressed by asbestos fibers [16]. These results indicate that oxidative DNA damage by asbestos is a potential cause of RCC onset. In consideration of these findings, asbestos exposure and BAP1 loss appeared to result in very rare cases of spousal RCC.
Although other environmental exposures, including infection, cannot be completely ruled out and limited epidemiological evidence exists for the occurrence of asbestos-triggered RCC, asbestos exposure and BAP1 loss might have contributed to concurrent occurrence of RCC with rhabdoid features in this married couple.
Future studies are necessary to elucidate the role of asbestos in the pathogenesis and progression of RCC with rhabdoid features.

Consent
Written informed consent was obtained from a son of the patients (married couple) for publication of this Case report and any accompanying images. A copy of the written consent is available for review by the Editor of this journal.