Rare histological subtypes of bladder cancer in clinical practice: a case series

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Non-urothelial tumors account for less than 5% of all bladder malignant neoplasms. The most common non-urothelial tumor is squamous cell carcinoma, often found in the Middle East (about 30% of all cases of bladder cancer – BC) due to the spread of schistosomiasis. The glandular type is the second most common non-urothelial morphological variant; it includes 5 tumor subtypes (intestinal, mucinous, signet ring cell, mixed, and adenocarcinoma not otherwise specified). The neuroendocrine variant is divided into 4 subgroups (small cell, large cell, highly differentiated, and paragangliomas), of which small cell is the most common, though still rare, and accounts for only about 1% of all BCs. The article presents the clinical cases of three rare BC subtypes: squamous cell, glandular, and neuroendocrine. In the first clinical case, a radical cure of a patient with signet ring cell BC was described: at the first stage, the bladder, prostate, and vesicles were removed with a cystoplasty using a small intestine segment according to the Bricker technique with an extended pelvic lymph node dissection; the second stage included 8 courses of adjuvant drug treatment according to the XELOX regimen. In the second clinical case, the treatment of the metastatic neuroendocrine BC was described using the following regimens: EP (etoposide + cisplatin), carboplatin + irinotecan, GemOx (gemcitabine + oxaliplatin). The third clinical case described a patient with bladder squamous cell carcinoma. The stage I treatment was based on the GC regimen; at stage II, the bladder, prostate, and vesicles were removed with intestinal orthotopic cystoplasty and extended lymph node dissection; due to progression revealed during the follow-up examination, the patient received another GC course. Although non-urothelial BCs are very rare, studies are currently being conducted on the effectiveness of immunotherapy and targeted therapy in treating this cohort of patients.

作者简介

Anna Paychadze

Hertsen Moscow Oncology Research Institute – branch of the National Medical Research Radiological Centre

Email: paiann@mail.ru
ORCID iD: 0000-0001-7912-8055

Cand. Sci. (Med.)

俄罗斯联邦, Moscow

Sofia Golubeva

Hertsen Moscow Oncology Research Institute – branch of the National Medical Research Radiological Centre

Email: Golu-sofya@ya.ru

врач-онколог отделения комбинированных методов лечения №1

俄罗斯联邦, Moscow

Milyausha Kamalova

Hertsen Moscow Oncology Research Institute – branch of the National Medical Research Radiological Centre

编辑信件的主要联系方式.
Email: milyausha.kamalova.97@mail.ru
ORCID iD: 0000-0003-0495-8585

Resident Physician

俄罗斯联邦, Moscow

参考

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2. Fig. 1. Pelvic computed tomography (CT) dated 10.09.2022: a contrast-enhancing mass with a pronounced diffusion restriction and axial dimensions of 31×21 mm.

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3. Fig. 2. Pelvic magnetic resonance imaging (MRI) dated 14.10.2021: tumor mass of irregular shape with ill-defined uneven contours with a mixed growth pattern. The size of the endophytic component is 40×21 mm, and the size of the exophytic component is 8×6 mm.

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4. Fig. 3. Bone scintigraphy dated 20.10.2021: multifocal metastatic bone lesions.

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5. Fig. 4. Pelvic MRI dated 14.10.2021 in comparison with MRI dated 27.12.2021. State after the 3rd course of drug treatment according to the EP regimen: tumor mass of irregular shape with ill-defined uneven contours with a mixed growth pattern up to 14×11 mm with an intraluminal component.

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6. Fig. 5. Pelvic MRI dated 27.12.2021 in comparison with MRI dated 24.03.2022. State after the 6th course of drug treatment according to the EP regimen: no tumor growth.

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7. Fig. 6. Pelvic MRI dated 07.06.2022. State after the 6th course of drug treatment according to the EP regimen. Monochemotherapy with etoposide is ongoing.

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8. Fig. 7. Pelvic MRI dated 07.06.2022 in comparison with pelvic MRI dated 18.08.2022. State after the 6th course of drug treatment according to the EP regimen. MCT with etoposide is ongoing. A rounded nodule with bulging contour appeared.

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9. Fig. 8. Pelvic MRI dated 18.08.2022 in comparison with pelvic CT dated 02.11.2022. State after 3 courses of drug treatment with carboplatin + irinotecan.

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10. Fig. 9. Abdominal CT scan dated 02.11.2022 in comparison with CT scan dated 11.01.22. Bilobar focal lesions of the liver: in S2 – up to 20×23 cm, at the border of S2|3 – up to 13×15 cm, in S6 – 8×11 mm.

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11. Fig. 10. Abdominal CT scan dated 02.11.2022 in comparison with CT scan dated 11.01.2022. Bilobar focal lesions of the liver: in S2 – up to 20×23 cm, at the border of S2|3 – up to 13×15 cm, in S6 – 8×11 mm.

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12. Fig. 11. Abdominal MRI of the abdomen, frontal view (T2-weighted image). A conglomerate of enlarged (>5 cm) lymph nodes in the para-aortic region on the right (arrow).

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