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Revision as of 15:22, 12 February 2016

Transitional cell carcinoma Microchapters

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Differentiating Transitional cell carcinoma from other Diseases

Epidemiology and Demographics

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Pathophysiology

Gross Pathology

The following table illustrates the findings on gross pathology for the subtypes of transitional cell carcinoma:[1][2][3]

Type Description

Non-invasive urothelial carcinoma

Invasive urothelial carcinoma

  • Large infiltrative mass or a multifocal, flat to papillary lesion with delicate fronds

Microscopic Pathology

Non-invasive urothelial carcinoma

  • Non-invasive urothelial carcinomas are only in the lining of the renal pelvis or ureter and have not grown deeper into the wall of the renal pelvis or ureter.

Invasive urothelial carcinoma

  • Invasive urothelial carcinomas grow from the lining of the renal pelvis or ureter into the deeper layers of the renal pelvis or ureter wall, such as lamina propria and muscularis.
  • Urothelial carcinomas with mixed epithelial features are invasive tumors that have different types of cells mixed with the cancer cells.
  • They occur less often than typical invasive urothelial carcinomas and are generally considered to be more aggressive.
  • The following table illustrates the findings on microscopic analysis for the subtypes of invasive transitional cell carcinoma:
Subtype Features on Histopathological Microscopic Analysis

Urothelial carcinomas with squamous differentiation

  • Have urothelial and squamous cells
  • Observed in 44% of renal pelvis tumors

Urothelial carcinomas with glandular differentiation

  • Presence of gland cells and true glandular spaces
  • Mucin production
  • Floating signet ring cells within the mucinous material

Micropapillary urothelial carcinomas

  • Have micropapillae
  • High grade neoplasm

Sarcomatoid urothelial carcinomas

  • Have cells that look like sarcoma
  • This aggressive carcinoma has often spread to lymph nodes and organs other than the renal pelvis or ureter when it is diagnosed

Nested variant of urothelial carcinomas

  • Have nests, which are groups of anaplastic cells with large nuclei
  • Very rare but aggressive

Microcystic urothelial carcinomas

  • Have cysts in them that can range in size from microscopic to 2 mm
  • Very rare

Lymphoepithelioma-like urothelial carcinomas

  • Have lymphatic tissue mixed with urothelial cells, or transitional cells
  • Very rare carcinoma
  • More common in men than women

Plasmacytoid and lymphoma-like urothelial carcinomas

  • Have tumor cells that look like lymphoma or plasmacytoma

Giant cell urothelial carcinomas

  • Have abnormally large cells with more than one nucleus.

Clear cell urothelial carcinomas

  • Have clear cells (cells with clear cytoplasm and a large nucleus).

Lipid cell variant of urothelial carcinomas

  • Have cells that are filled with fat

Undifferentiated variant of urothelial carcinomas

  • Have cells that don’t have any clear features and don’t look like any other type of cell (they are undifferentiated).

Urothelial carcinomas with trophoblastic differentiation

  • Presence of cells that look like trophoblasts
  • Human chorionic gonadotropin production within the cells

Grading

According to the WHO grading criteria, there are two grades of transitional cell carcinoma based on the degree of cellular differentiation:

Grade Description

Low grade

  • Tumors with the least degree of cellular anaplasia compatible with a diagnosis of malignancy

High grade

  • Tumors with the most severe degrees of cellular anaplasia

References

  1. Cheng L, Cheville JC, Neumann RM, Bostwick DG (2000). "Flat intraepithelial lesions of the urinary bladder". Cancer. 88 (3): 625–31. PMID 10649257.
  2. Cheng L, Cheville JC, Neumann RM, Bostwick DG (1999). "Natural history of urothelial dysplasia of the bladder". Am J Surg Pathol. 23 (4): 443–7. PMID 10199474.
  3. Pons F, Orsola A, Morote J, Bellmunt J (2011). "Variant forms of bladder cancer: basic considerations on treatment approaches". Curr Oncol Rep. 13 (3): 216–21. doi:10.1007/s11912-011-0161-4. PMID 21360040.

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