Large cell neuroendocrine carcinoma (LCNEC) of the urinary bladder: a case report
© Colarossi et al.; licensee BioMed Central Ltd. 2013
Received: 16 January 2013
Accepted: 30 January 2013
Published: 4 February 2013
Neuroendocrine carcinoma of the urinary bladder is a rare entity, accounting less then 1% of urinary bladder malignancies. The vast majority of the neuroendocrine carcinoma of the urinary bladder is represented by small cell neuroendocrine carcinoma while just few cases of large cell neuroendocrine carcinoma (LCNEC) have been reported. In this cases report we describe a rare case of primary bladder LCNEC.
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Neuroendocrine carcinoma of the urinary bladder is a rare entity, accounting less than 1% of urinary bladder malignancies . The vast majority of the neuroendocrine carcinomas of the urinary bladder is represented by small cell neuroendocrine carcinoma while just few cases of large cell neuroendocrine carcinoma (LCNEC) have been reported [1–9].
LCNEC was first described by Travis  in the lung but cases of LCNEC were reported in other organs like uterus, thymus, stomach, bile duct, larynx, parotid gland, prostate, kidney, and cervix [11, 12].
In this cases report we describe a rare cases of primary bladder LCNEC.
The patient was then treated with etoposide and cisplatin for 4 cycles. Reduction of the tumor and of the mesenteric lymph nodes size were seen at the end of the 4th cycle in December 2011. In January 2012 the patient underwent cystectomy with histero-annessectomy and lymphadenectomy in a different institution. At microscopic examination the diagnosis of LNEC was confirmed but area of conventional urothelial carcinoma were also seen associated with large amount of necrosis. The tumor showed infiltration of the perivesical tissue (pT3b) and metastasis were present in 5 right hypogastric lymph nodes (pN2) and in 2 common iliac lymph nodes (M1).
Following surgery, patient underwent a 5th cycle of chemotherapy with etoposide and cisplatin and she died on March 2012, seven months after the diagnosis.
Neuroendocrine tumors of the urinary bladder are relatively rare and include carcinoids, large cell neuroendocrine carcinomas and small cell neuroendocrine carcinomas, the latter being by far the most common. LCNEC was first described in the lung by Travis , as well as the criteria for its diagnosis. These include the presence of polygonal large cells with a low nuclear/cytoplasmic ratio, coarse nuclear chromatin and evident nucleoli, high mitotic ratio (>10 mitoses/ 10 HPF) and immunohistochemical or ultrastructural evidence of neuroendocrine differentiation.
Only few cases of LCNEC are present in the literature and most of them showing mixed histology, including the present case. In our case, areas of LCNEC and urothelial carcinoma were evident while in other reported cases were described areas of LCNEC mixed with a squamous cell or adenocarcinoma component. This is in line with the hypothesis that neuroendocrine cells originate from stem cells suggesting a common clonal origin of the neuroendocrine, urothelial, squamous or adenocarcinoma component .
Interestingly, around 30% of cases of small cell carcinoma or the urinary bladder are positive for TTF-1  while no evidence of expression of TTF-1 was found in LCNEC in the literature and in the present case.
In addition, to our knowledge, this is the first case in the literature of primary LCNEC of the bladder with known status of EGFR.
In our case, as well as in most of the described cases, tumor showed a very rapid local growth in few months, and this might be one of the important clinical manifestations of this rare tumor.
Recognition of this rare entity could be significant considering its poor outcome and differential diagnosis considerations. The differential diagnosis of primary LCNEC includes metastatic LCNEC, extension from poorly differentiated prostatic carcinomas, high grade urothelial carcinoma, small cell neuroendocrine carcinoma and lymphoma.
Written informed consent was obtained from the patient 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 this journal.
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