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Histologic Variants of Urothelial Carcinoma

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Histologic Variants of Urothelial Carcinoma Medical College of Georgia 12/04/2006 Jeremy S. Miller, MD Histologic variants of urothelial carcinoma: differential ... – PowerPoint PPT presentation

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Title: Histologic Variants of Urothelial Carcinoma


1
Histologic Variants of Urothelial Carcinoma
  • Medical College of Georgia
  • 12/04/2006

Jeremy S. Miller, MD
2
Histologic variants of urothelial carcinoma
differential diagnosis and clinical implications
Antonio Lopez-Beltran MD and Liang Cheng
MD Cordoba University Medical School, Cordoba,
Spain Indiana University School of Medicine,
Indiana
Human Pathology (November 2006) Volume 37,
1371-1388
3
Why is this important?
  • A wide array of histologic variants of urothelial
    carcinoma have been recognized in recent years
  • The principal danger is the misinterpretation of
    these cancer variants as benign
  • Also, some variants require a specific
    therapeutic approach

4
Background
  • Urothelial carcinoma (TCC) is the most common
    tumor of the urinary bladder (90 of tumors)
  • Propensity for divergent differentiation
  • 1. Squamous 2. Glandular
  • A variety of histologic patterns can be seen in
    an individual TCC, mimicking the following benign
    lesions
  • Brunns nests, cystitis cystica and glandularis
  • Inverted papilloma
  • Paraganglioma
  • Nephrogenic metaplasia (aka nephrogenic adenoma)

5
Brunns nests
6
Cystitis cystica
7
Cystitis glandularis
8
Intestinal metaplasia
9
Inverted papilloma
10
Paraganglioma
11
Nephrogenic metaplasia
12
TCC Variants
  • Nested
  • Inverted papilloma-like
  • Micropapillary
  • Microcystic
  • Lymphoepithelioma-like (LELC)
  • Plasmacytoid
  • Clear cell (glycogen-rich)
  • Lipoid cell
  • TCC w/ syncytiotrophoblastic giant cells
  • Sarcomatoid carcinoma
  • Small cell
  • Mixed (Specify type and )
  • Large cell undifferentiated
  • TCC w/ unusual stromal reaction

13
Nested variant
  • Aggressive
  • Male predominance
  • Deceptively benign closely resembles Brunns
    nests in the lamina propria
  • Majority of lesion often shows little nuclear
    atypia however, malignant cytology is a
    requirement and is often most apparent deep in
    the nests

14
Nested pattern TCC
15
Nested pattern TCC
16
Nested variant
  • Differential Diagnosis
  • Hyperplasia of Brunns nests
  • Cystitis cystica, glandularis
  • Inverted papilloma
  • Nephrogenic metaplasia
  • Carcinoid tumor
  • Paraganglioma

17
Inverted papilloma-like variant
  • By definition, this is an inverted papilloma with
    significant nuclear pleomorphism, mitotic
    figures, architectural abnormalities, and high
    proliferation index (PI) via Ki-67 labeling
  • Inverted papilloma with atypia As above with
    rare mitoses and low PI via Ki-67
  • Prognosis unclear however, likelihood of
    metastases appears to be minimal

18
Inverted pattern TCC
19
Inverted pattern TCC
20
Micropapillary variant
  • Male predominance mean age 66 years
  • Resembles serous carcinoma of the ovary
  • Extremely rare for this pattern to be found alone
  • When present as gt 10 of the overall pattern,
    muscular or vascular invasion is likely (and
    metastases are the norm)
  • Cells have reversed polarity
  • MUC1 expression on the basal aspect of cells is
    both specific diagnostically and responsible for
    the high rate of metastases

21
Micropapillary pattern TCC
22
Micropapillary pattern TCC
23
Micropapillary pattern TCC
24
Micropapillary pattern TCC
25
Micropapillary pattern TCC, metastatic to lymph
node
26
Micropapillary variant
  • Differential Diagnosis
  • Metastatic serous carcinoma (CK20-)
  • vs. micropapillary TCC (CK20)
  • Metastatic mesothelioma (LeuM1 CD15 -)
  • vs. micropapillary TCC (LeuM1 CD15 )

27
Microcystic variant
  • Formation of microcysts, macrocysts, and tubular
    structures that often contain necrotic debris or
    mucin
  • Prognosis similar to standard TCC
  • Preferred name is now
  • Urothelial carcinoma with gland-like lumina

28
Microcystic pattern TCC
29
Bladder Adenocarcinoma
30
Microcystic variant
  • Differential diagnosis
  • Adenocarcinoma
  • Florid cystitis cystica, glandularis
  • Nephrogenic metaplasia
  • Metastatic prostate adenocarcinoma
  • Use PSA, PAP

31
Lymphoepithelioma-like variant (LELC)
  • Male predominance mean age 69 years
  • Resembles lymphoepithelioma of nasopharynx (but
    not related to EBV)
  • Nests, sheets, and cords of cells with
    significant pleomorphism in a background of a
    polyclonal lymphoid stroma
  • High grade, but responsive to high-dose
    chemotherapy

32
LELC
33
LELC
34
SCCA, bladder
35
Lymphoepithelioma-like variant (LELC)
  • Differential diagnosis
  • Poorly-differentiated TCC with lymphoid stroma
  • Poorly-differentiated SCCA
  • Neither of the above will have the syncytial
    pattern required for a diagnosis of LELC

36
Plasmacytoid variant
  • Male predominance mean age 58 years
  • Diffuse, high-grade and stage tumors composed of
    medium-sized cells with eosinophilic cytoplasm
    and eccentric nuclei
  • Cells keratin positive, CD138 negative
  • Mean survival less than 2 years

37
Plasmacytoid variant
38
Pankeratin
Plasmacytoid variant
39
Lymphoma, bladder
40
Plasmacytoid variant
  • Differential diagnosis
  • Lymphoma (predominantly plasmacytoid type)
  • Myeloma
  • Staining with epithelial markers required

41
Clear cell (glycogen-rich) variant
  • Clear cell change is common in TCC (reportedly
    present in over 60 of all cases)
  • Cytoplasmic clearing is a result of abundant
    glycogen
  • Clear cell (glycogen-rich) variant is used when
    this is the predominant pattern and the cells
    stain for CK7

42
Clear cell (glycogen-rich) variant
43
PAS stain
Clear cell (glycogen-rich) variant
44
Clear cell adenocarcinoma, bladder
45
Clear cell (glycogen-rich) variant
  • Differential diagnosis
  • Clear cell adenocarcinoma
  • Metastatic clear cell carcinoma of the kidney
  • Paraganglioma

46
Lipoid cell variant
  • Male predominance mean age 74 years
  • High-grade and -stage urothelial carcinomas with
    areas of cells resembling signet ring lipoblasts
  • Lipoid cells must stain for epithelial markers

47
Lipoid cell variant
48
Lipoid cell variant
  • Differential diagnosis
  • Carcinosarcoma with liposarcomatous component
  • Reactivity of the lipoid cells for epithelial
    markers can be used in this setting

49
TCC with syncytiotrophoblastic giant cells
  • Syncytiotrophoblastic giant cells, which produce
    ß-HCG to varying degrees, can be found in up to
    10 of TCCs
  • Radiation treatment is useful
  • Serum levels of ß-HCG are used to monitor
    response to radiation therapy

50
TCC with syncytiotrophoblastic giant cells
51
Choriocarcinoma, metastatic to bladder
52
TCC with osteoclast-like giant cells
53
TCC with syncytiotrophoblastic giant cells
  • Differential Diagnosis
  • Choriocarcinoma (ß-HCG and HPL)
  • Metastatic - uncommon
  • Primary - exceedingly rare (lt 10 cases reported)
  • Sarcomatoid carcinoma of bladder with
    trophoblastic differentiation
  • TCC with osteoclast-like giant cells

54
Sarcomatoid carcinoma
  • Mean age 66 years
  • Biphasic malignant neoplasms with both epithelial
    and mesenchymal components
  • Also known by many previous and current names
  • Carcinosarcoma
  • Pseudosarcomatous TCC
  • MMMT
  • Spindle cell carcinoma
  • Metaplastic carcinoma
  • Previous history of carcinoma treated with
    radiation or cyclophosphamide is common
  • Whether or not the tumor harbors heterologous
    elements should be a component of the final report

55
Sarcomatoid carcinoma
  • Epithelial component
  • Urothelium
  • Squamous
  • Glandular
  • Small cell
  • Large cell neuroendocrine (rare)
  • Mesenchymal component
  • Undifferentiated high grade spindle cell (most
    common)
  • Osteosarcoma, chondrosarcoma, rhabdomyosarcoma,
    leiomyosarcoma, liposarcoma, angiosarcoma

56
Sarcomatoid carcinoma
57
Leiomyosarcoma
58
Sarcomatoid carcinoma
  • Differential Diagnosis
  • TCC with pseudosarcomatous stroma
  • Reactive, polyclonal stroma
  • Sarcoma
  • Primarily leiomyosarcoma
  • Inflammatory myofibroblastic tumor (ALK-1)
  • Neurofibroma

59
Small cell variant
  • Male predominance mean age 66 years
  • Malignant cells with neuroendocrine features
  • Mitoses and necrosis common
  • Recent molecular evidence has indicated that
    small cell carcinoma and TCC are derived from the
    same clonal population most authors now
    consider this a variant of TCC rather than a
    separate entity

60
Small cell variant
  • Dismal prognosis, regardless of treatment
  • Recent study of 64 patients
  • 98 had muscle-invasive disease at presentation
  • 66 had lymph node metastases at cystectomy
  • 32 pure, 68 mixed with TCC, SCCA, others
  • Genetically unstable commonly exhibit multiple
    cytogenetic abnormalities
  • 3 year survival is 23

61
Small cell variant
62
Small cell variant
  • Differential diagnosis
  • Metastatic small cell carcinoma from another site
    (predominantly lung)
  • Lymphoma
  • LELC
  • Plasmacytoid variant of TCC

63
Mixed variant
  • Squamous and/or glandular differentiation is
    found in over 20 of TCCs
  • These mixed variants have a less favorable
    response to therapy, and have a higher recurrence
    rate

64
Squamous differentiation (elsewhere this tumor
had TCC)
65
Glandular differentiation (elsewhere this tumor
had TCC)
66
Mixed variant
  • Differential diagnosis
  • Squamous cell carcinoma, bladder
  • Adenocarcinoma, bladder
  • Metastases
  • All of the above will have, by definition, no
    urothelial component to the tumor

67
Large cell undifferentiated
  • Rare, high-grade and stage tumors with large
    undifferentiated cells
  • Reactivity with epithelial and mesenchymal
    markers are inconsistent
  • Prognosis extremely poor, regardless of therapy

68
Large cell undifferentiated carcinoma
69
Large cell undifferentiated
  • Differential diagnosis
  • Sarcomatoid carcinoma with giant cells
  • Metastatic large cell carcinoma (often lung
    primary)
  • TCC with syncytiotrophoblastic giant cells
  • TCC with osteoclast-like giant cells

70
Unusual stromal reaction
  • Invasive TCCs often have a significant stromal
    reaction
  • Osseous and/or chondroid metaplasia can sometimes
    be found, but will be histologically benign
  • Osteoclast-like giant cells have been noted in a
    subset of TCCs these seem to have no effect on
    prognosis
  • Intense mononuclear inflammation is indicative of
    a better prognosis when compared to TCCs with no
    inflammation

71
Pseudosarcomatous stroma
Osseus metaplasia
Osteoclast-like giant cells
Lymphoid infiltrate
72
Unusual stromal reaction
  • Differential diagnosis
  • Sarcoma
  • Sarcomatoid carcinoma
  • TCC with syncytiotrophoblastic giant cells
  • LELC

73
Rare variants
  • Some TCCs mimic morphology usually found in other
    organs
  • Infiltrating lobular carcinoma of the breast
  • Diffuse gastric carcinoma
  • All express bladder markers rather than breast or
    gastric markers

74
TCC mimicking lobular carcinoma of the breast
75
Summary TCC variants
  • POOR PROGNOSIS/ AGGRESSIVE
  • Nested
  • Micropapillary
  • Plasmacytoid
  • Lipoid cell
  • Sarcomatoid carcinoma
  • Small cell
  • Large cell undifferentiated
  • SIMILAR PROGNOSIS TO TCC/ RECOGNITION IS KEY
  • Inverted papilloma-like
  • Microcystic
  • Lymphoepithelioma-like (LELC)
  • Clear cell (glycogen-rich)
  • TCC w/ syncytiotrophoblastic giant cells
  • Mixed (Specify type and )
  • TCC w/ unusual stromal reaction
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