Open Access

Lymphoepithelioma-like carcinoma of the urinary bladder: a case report and review of the literature

BMC Research Notes20147:779

https://doi.org/10.1186/1756-0500-7-779

Received: 13 March 2014

Accepted: 18 September 2014

Published: 4 November 2014

Abstract

Background

Lymphoepithelioma-like carcinoma is an undifferentiated carcinoma with histological features similar to undifferentiated, non-keratinizing carcinoma of the nasopharynx. Lymphoepithelioma-like carcinoma of the urinary bladder is uncommon with a reported incidence of 0.3%– 1.3% of all bladder cancer. We report a Japanese case of predominant lymphoepithelioma-like carcinoma of the urinary bladder and review all of the English literature after performing a pooled analysis of the cases including the present one.

Case presentation

An 83-year-old Japanese man was introduced to our department with the chief complaint of macroscopic hematuria. Cystoscopy demonstrated a thumb tip-sized bladder tumor at the trigone. The patient underwent a transurethral resection of the bladder tumor. The pathological examination showed predominant lymphoepithelioma-like carcinoma of the urinary bladder with urothelial carcinoma. The patient was diagnosed with muscle invasive lymphoepithelioma-like carcinoma of the urinary bladder and was treated with concurrent chemoradiotherapy. The patient is under observation with regular clinical follow-up and remains well after 12 months, with no evidence of disease recurrence. The reports of 93 patients including the present one of lymphoepithelioma-like carcinoma of the urinary bladder from the English literature were collected between 1991 and 2014. Patients were evaluated for clinicopathological findings. Outcome resulted as follows: 59 patients (67%) did not show evidence of disease, 14 (17%) died of disease, 5 (6%) was alive with metastases, and 9 (10%) died for causes unrelated to the primary disease. Cause-specific survival rate resulted 83%. The overall patients were divided into three groups (pure, predominant and focal) according to the lymphoepithelioma-like carcinoma of the urinary bladder classification of Amin et al.

Conclusions

Because lymphoepithelioma-like carcinoma of the urinary bladder is more sensitive to both chemotherapy and radiotherapy than conventional urothelial carcinoma, radical cystectomy may not be necessary for all patients with muscle invasive lymphoepithelioma-like carcinoma of the urinary bladder. Therefore, pathological information may be useful in selecting patients suitable for bladder-preservation treatment. On the other hand, the apparently more aggressive nature of focal lymphoepithelioma-like carcinoma of the urinary bladder suggests that these patients are probably best managed with radical cystectomy and adjuvant treatment.

Keywords

Lymphoepithelioma-like carcinoma Urinary bladder Bladder-preservation treatment

Background

Undifferentiated, non-keratinizing carcinoma with prominent lymphocytic infiltrate arising outside of the nasopharynx is called lymphoepithelioma-like carcinoma (LELC). Although LELC occurs in organs, such as salivary glands, uterine cervix, thymus, lung, skin, stomach, and breast, its occurrence in the urinary system is very rare. LELC of the urinary bladder (LELCB) has a reported incidence of 0.3%– 1.3% of all bladder cancer [13]. Contrary to nasopharynx cases, no relationship with Epstein-Barr virus has been reported. According to the lymphoepithelioma component, these tumors were classified as pure (100%), predominant (≥50%), and focal (<50%), advocated by Amin et al. [4].

Because of the small number of cases reported in the literature, there are no clear guidelines for the treatment of LELCB. Several reports suggest that, unlike conventional urothelial carcinoma and focal LELCB, the pure and predominant LELCB, irrespective of stage, are sensitive to chemotherapy and radiotherapy. This observation raises the potential of salvaging bladder function in patients with these subtypes [1, 2, 4]. This advantage is lost when the urothelial elements predominate.

Case presentation

An 83-year-old Japanese man was introduced to our department with the chief complaint of macroscopic hematuria. There was a past medical history of hepatitis B and hepatocellular carcinoma treated with radiofrequency ablation, but no history of urological problems. Physical examination and vital signs were unremarkable.

Urinalysis showed combined hematuria and pyuria, but urine culture was sterile. Urine cytology indicated atypical cells. Abnormal hematological findings include leukocytosis (WBC count: 15,700/μl) and eosinophilia (12%). The serum IgE level was 9.8 IU/ml (normal <173 IU/ml).Cystoscopy demonstrated a thumb tip-sized bladder tumor at the trigone (Figure 1) and papillary mucosa at the left lateral wall. Contrast-enhanced magnetic resonance imaging (MRI) showed a 20 × 17 × 15 mm bladder tumor at the trigone and muscle invasion in the bladder (Figure 2). Computed tomography (CT) revealed no distant metastases. The patient underwent transurethral resection of the bladder tumor (TURBT). Histopathological examination revealed that 90% of the volume of the tumor was LELC marked by syncytial growth pattern (Figure 3), heavy lymphocytic infiltrate, necrosis, brisk mitosis and muscle invasion. The epithelial cells expressed CK7 and CK34βE12, and the lymphocytes CD3 and CD20 (Figure 4). The rest of the tumor was composed of non-invasive urothelial carcinoma.
Figure 1

Cystoscopy revealed a thumb tip-sized bladder tumor at the trigone. The tumor was solid and broad-based. asterisk, flexible cystoscope; arrow, neck of bladder

Figure 2

Contrast-enhanced magnetic resonance imaging (sagittal image) showed a bladder tumor (arrow) at the trigone, 20 × 17 × 15 mm in size, with muscle invasion.

Figure 3

Microscopic findings (left, ×100; right, ×400). Lymphoepithelioma-like carcinoma, syncytial pattern with prominent lymphocytic infiltrate and lymphoepithelioma-like carcinoma with urothelial carcinoma.

Figure 4

Immunohistochemical findings of CK7, CK34βE12, CD3, and CD20. The epithelial component revealed overexpression of CK7. Focal staining for CK34βE12 was detected. Positive staining with antibodies against CD3 and CD20 showed abundant T-lymphocytes and less B-lymphocytes, respectively.

The patient received concurrent chemoradiotherapy. The chemotherapy regimen included gemcitabine administered at 1000 mg/m2 on Days 1 and 8 and cisplatin 70 mg/m2 on Day 1 of a 21-day cycle. Radiotherapy, 60 Gy in total, was started on Day 1, concurrently with chemotherapy.

Ten months after his initial visit to our department, the patient underwent second TURBT for evaluation of pathological effect. No viable cancer cells were detected in the bladder specimens, including the muscle layer. At the time of this writing, the patient is under observation with regular clinical follow-up and remains well after 12 months, with no evidence of disease recurrence.

Materials and methods

On the basis of the review from 1991 to 2002 by Porcaro AB et al. [5], we added subsequent LELCB reports to the review and summarized. Conduct of this study conformed to the Declaration of Helsinki, and was approved by our institutional ethical committee (Institutional Review Board of Onomichi General hospital). The reports of 93 patients including the present one of LELCB from the English literature were collected from 1991 to 2014, as shown in Table 1[123]. Patients were evaluated for age, sex, primary and adjuvant treatments, pathological stage, follow-up and outcome, and cause-specific survival. Patients underwent cystoscopy and transurethral resection of the tumor for both biopsy or complete removal of the mass. Tumor specimens were evaluated for local pathological stage (available in 92 cases), histological subtype according to the classification of Amin et al. for LELCB. LELCB was classified as pure when 100% of the tumor showed lymphoepithelioma-like carcinoma pattern, and predominant or focal when associated with usual urothelial carcinoma, adenocarcinoma, or squamous cell carcinoma. Mixed subtype in Table 2 was used synonymously with predominant or focal [6]. Primary treatments performed included TURBT, partial cystectomy, and radical cystectomy. Adjuvant treatments, when performed, included several courses of systemic multiagent chemotherapy with MVAC (methotrexate, vinblastine, doxorubicin, and cisplatin) or GC (gemcitabine, cisplatin), as well as intravesical chemotherapy with doxorubicin or bacillus Calmette-Guerin, and radiotherapy.
Table 1

Reports of lymphoepithelioma-like carcinoma of the urinay bladder from the English literature including the present case

Case no.

Reference

Year

Sex

Age

Chief complaint

Type

Stage

Treatment

Follow-up

Outcome

1

Zukerberg

1991

M

76

NA

PU

NA

TURBT, RT

NA

NA

2

Young

1993

M

81

NA

PU

T3

PC, CH

41

DOD

3

Dinney

1993

M

52

GH

PU

T2

TURBT, CH

72

NED

4

Dinney

1993

M

68

GH

PU

T2

TURBT, CH

60

NED

5

Dinney

1993

M

63

NA

PU

T2

TURBT, CH

11

NED

6

Amin

1994

M

52

GH

PU

T2

TURBT, CH

72

NED

7

Amin

1994

M

68

GH

PU

T2

TURBT, CH

60

NED

8

Amin

1994

M

63

GH

PU

T2

TURBT, CH

11

NED

9

Amin

1994

F

71

GH

PR

T2

TURBT, CH

9

NED

10

Amin

1994

F

67

GH

PR

T3

PC, RT

36

NED

11

Amin

1994

M

55

GH

PR

T2

RC

10

NED

12

Amin

1994

M

71

GH

PR

T2

RC

6

NED

13

Amin

1994

F

79

GH

PR

T3

RC

2

NED

14

Amin

1994

M

78

GH

F

T2

RC, CH

84

DOD

15

Amin

1994

M

66

GH

F

T3

RC

6

DOD

16

Amin

1994

M

68

GH

F

T1

RC

0

DWD

17

Bianchini

1996

M

72

NA

PU

T3

RC, CH

29

NED

18

Holmäng

1998

F

61

GH

PU

T2

TURBT, RT

216

DWD

19

Holmäng

1998

M

78

GH

PU

T1

TURBT, RT

13

DWD

20

Holmäng

1998

M

65

GH

PU

T2

TURBT

24

NED

21

Holmäng

1998

F

71

GH

PR

T3

TURBT, RT

21

DWD

22

Holmäng

1998

F

60

GH

PR

T3

RC, RT

104

NED

23

Holmäng

1998

F

65

GH

PR

T3

PC

76

NED

24

Holmäng

1998

F

84

GH

F

T1

TURBT

66

DOD

25

Holmäng

1998

M

72

GH

F

T3

RC, RT

68

DOD

26

Holmäng

1998

M

71

GH

F

T3

TURBT, RT

9

DOD

27

Constantinides

2001

M

NA

GH, Urgency

PU

T2

TURBT, CH

34

NED

28

Constantinides

2001

M

NA

GH, Urgency

PU

T1

TURBT, IV-CH

28

NED

29

Constantinides

2001

M

NA

GH, Urgency

PR

T2

RC

32

NED

30

Lopez-B

2001

F

69

NA

PU

T2

TURBT, CH

21

NED

31

Lopez-B

2001

M

72

NA

PU

T3

RC

32

NED

32

Lopez-B

2001

M

81

NA

PU

T2

TURBT, CH

47

NED

33

Lopez-B

2001

M

69

NA

PR

T2

TURBT

22

NED

34

Lopez-B

2001

F

67

NA

PR

T2

RC

22

NED

35

Lopez-B

2001

M

73

NA

PR

T3

RC

37

NED

36

Lopez-B

2001

M

82

NA

PR

T2

TURBT

49

NED

37

Lopez-B

2001

M

74

NA

PR

T2

TURBT

25

AWM

38

Lopez-B

2001

F

81

NA

PR

T2

TURBT

44

DOD

39

Lopez-B

2001

M

78

NA

F

T2

TURBT

3

DOD

40

Lopez-B

2001

F

58

NA

F

T2

RC

19

DOD

41

Lopez-B

2001

M

71

NA

F

T2

TURBT

30

DOD

42

Lopez-B

2001

M

69

NA

F

T3

RC

18

DOD

43

Ward

2002

M

61

GH

PR

T2

TURBT

NA

NA

44

Porcaro

2003

M

72

NA

PR

T2

TURBT

17

NED

45

Chen

2003

M

73

GH

PU

T3

RC, CH

26

NED

46

Chen

2003

M

63

GH

PU

T1

TURBT, IV-CH

26

NED

47

Izuquierdo

2004

M

77

GH

PU

T2

TURBT, RT

39

NED

48

Izuquierdo

2004

F

82

GH

PR

T2

TURBT

36

NED

49

Izuquierdo

2004

M

74

GH

F

T2

TURBT, RT

54

NED

50

Guresci

2005

M

90

GH

PR

T3

TURBT

NA

NA

51

Abascal

2005

M

54

GH

NA

T3

NA

NA

NA

52

Yaqoob

2005

F

55

GH, Miction pain

NA

T2

TURBT

NA

NA

53

Mayer

2007

M

57

GH

PU

T1

RC

36

NED

54

Tamas

2007

NA

NA

NA

PU

T3

PC

23

AWM

55

Tamas

2007

NA

NA

NA

PU

T2

RC

40

NED

56

Tamas

2007

NA

NA

NA

PU

T4

RC, RT

36

NED

57

Tamas

2007

NA

NA

NA

PU

T3

RC

42

NED

58

Tamas

2007

NA

NA

NA

PU

T2

RC

46

NED

59

Tamas

2007

NA

NA

NA

PU

T4

RC, CH

29

NED

60

Tamas

2007

NA

NA

NA

PU

T3

RC

23

NED

61

Tamas

2007

NA

NA

NA

PU

T2

RC

3

DWD

62

Tamas

2007

NA

NA

NA

PU

T2

TURBT, CH, RT

17

NED

63

Tamas

2007

NA

NA

NA

PU

T2

TURBT, Thermal, CH

4

NED

64

Tamas

2007

NA

NA

NA

PU

T1

TURBT, RT

6

NED

65

Tamas

2007

NA

NA

NA

PU

T3

RC

4

NED

66

Tamas

2007

NA

NA

NA

PU

T2

TURBT, RT, CH

65

DWD

67

Tamas

2007

NA

NA

NA

PU

T1

TURBT, IV-CH

38

NED

68

Tamas

2007

NA

NA

NA

PU

T1

TURBT

48

DWD

69

Tamas

2007

NA

NA

NA

PU

T2

RC

2

NED

70

Tamas

2007

NA

NA

NA

Mixed

T3

RC

55

NED

71

Tamas

2007

NA

NA

NA

Mixed

T2

TURBT, RT, CH

24

NED

72

Tamas

2007

NA

NA

NA

Mixed

T2

PC

10

NED

73

Tamas

2007

NA

NA

NA

Mixed

T2

TURBT

4

AWM

74

Tamas

2007

NA

NA

NA

Mixed

T1

TURBT, CH

6

NED

75

Tamas

2007

NA

NA

NA

Mixed

T1

TURBT

42

DWD

76

Tamas

2007

NA

NA

NA

Mixed

T1

RC

9

NED

77

Tamas

2007

NA

NA

NA

Mixed

T2

TURBT, CH

2

NED

78

Tamas

2007

NA

NA

NA

Mixed

T2

TURBT, RT, CH

8

AWM

79

Tamas

2007

NA

NA

NA

Mixed

T1

RC

18

DOD

80

Tamas

2007

NA

NA

NA

Mixed

T3

RC

5

AWM

81

Tamas

2007

NA

NA

NA

Mixed

T2

PC

2

NED

82

Singh

2009

M

69

GH

PU

T2

RC

12

NED

83

Trabelsi

2009

M

58

GH

NA

T2

RC

NA

NA

84

Yun

2010

F

78

GH

PR

T1

TURBT

8

NED

85

Kozyrakis

2011

M

72

GH

PR

T2

TURBT, RT

72

NED

86

Kozyrakis

2011

M

75

GH

PR

T3

RC, CH

26

NED

87

Kozyrakis

2011

F

80

GH

PR

T2

TURBT, RT

13

NED

88

Kozyrakis

2011

F

69

GH

PR

T3

RC, CH

34

DWD

89

Kozyrakis

2011

M

70

GH

F

T2

TURBT

14

DOD

90

Kozyrakis

2011

M

72

GH

F

T2

TURBT, RT, CH

27

DOD

91

Pantelides

2012

M

64

GH

PU

T2

TURBT, CH

6

NED

92

Mori

2013

M

70

GH

PR

T2

RC

10

NED

93

Present case

2014

M

83

GH

PR

T2

TURBT, CH, RT

12

NED

NA Not available, GH Gross hematuria, PU pure, PR Predominant, F Focal, TURBT Transurethral resection of the bladder tumor, PC Partial cystectomy, RC Radical cystectomy, CH Chemotherapy, RT Radiotherapy, IV-CH Intravesical chemotherapy, NED Not evidence of disease, DOD Died of disease, DWD Died without disease, AWM Alive with metastases.

Table 2

Lymphoepithelioma-like carcinoma of the urinary bladder: clinical and pathological results in 93 cases

Features

 

Patient population

Sex

(n = 65)

 

  Male

 

48 (74%)

  Female

 

17 (26%)

Age

(n = 62)

 

  Mean

 

70.0

  Range

 

52-90

Chief complaint

(n = 35)

 

  GH

 

31 (88%)

  GH and Urgency

 

3 (9%)

  GH and Miction pain

 

1 (3%)

Histology

(n = 90)

 

  Pure

 

39 (43%)

  Predominant

 

26 (29%)

  Focal

 

13 (15%)

  Mixed

 

12 (13%)

Pathological stage (T)

(n = 92)

 

  T1

 

14 (15%)

  T2

 

52 (56%)

  T3

 

24 (27%)

  T4

 

2 (2%)

Primary treatment

(n = 92)

 

  TURBT

 

51 (55%)

  Partial cystectomy

 

6 (7%)

  Radical cystectomy

 

35 (38%)

Adjuvant treatment

(n = 92)

 

  Systemic chemotherapy

 

21 (23%)

  Radiotherapy

 

14 (15%)

  Chemoradiotherapy

 

6 (7%)

  Intravesical chemotherapy

 

3 (3%)

  Not performed

 

48 (52%)

Follow-up

(n = 87)

 

  Mean

 

30.4 (months)

  Range

 

0-216 (months)

Outcome

(n = 87)

 

  Not evidence of disease (NED)

 

59 (67%)

  Died of disease (DOD)

 

14 (17%)

  Died without disease (DWD)

 

9 (10%)

  Alive with metastases (AWM)

 

5 (6%)

Cause-specific survival rate

 

83%

GH Gross hematuria, TURBT Transurethral resection of the bladder tumor.

The overall patient population was separated into 3 groups according to the LELCB classification of Amin et al. Each group was evaluated for the same clinical, pathological features as described previously for the overall population group.

Results

As shown in Table 1, 93 patients with LELCB were reported from 1991 to 2014. Table 2 shows the features of the overall patient population which included 48 males and 17 females. Mean age was 70.0 years (range: 52–90). Gross hematuria (GH) was seen in all available patients with presenting symptoms. LELCB histological subtypes resulted pure in 39 cases (43%), predominant in 26 (29%), focal in 13 (15%), and mixed in 12 (13%). Patients with pT2 and pT3 together accounted for 83% of the patient population. Primary treatments included TURBT in 51 patients (55%), partial cystectomy in 6 (7%), and radical cystectomy in 35 (38%). Adjuvant treatment, which was not performed in 48 cases (52%), included systemic chemotherapy in 21 (23%), radiotherapy in 14 (15%), chemoradiotherapy in 6 (7%), and intravesical chemotherapy in 3 (3%). Outcome resulted as follows: 59 patients (67%) did not show evidence of disease, 14 (17%) died of disease, 5 (6%) was alive with metastases, and 9 (10%) died for causes unrelated to the primary disease. Cause-specific survival rate resulted 83% in the overall patient population.

Table 3 shows the results related to the three groups of patients with LELCB according to their histological classification: pure (group 1), predominant (group 2), and focal (group 3). Mean age resulted about 70 years in all groups. Pathological stage T2 and T3 together was detected in 76–97% of patients in each group. More than 90% of patients underwent TURBT or radical cystectomy as the primary treatment in all groups. Adjuvant treatment was as follows: Systemic chemotherapy was performed in 15 patients (38%) of the group 1, 3 (12%) of the group 2, and 1 (8%) of the group 3. Radiation was performed in 6 patients (16%) of the group 1, 5 (19%) of the group 2, and 3 (23%) of the group 3. Chemoradiation was done as adjuvant treatment in 2 patients (5%) of the group 1, 1 (4%) of the group 2, and 1 (8%) of the group 3. Intravesical chemotherapy was performed in 3 patients (8%) of the group 1. Adjuvant treatment was not performed in 13 patients (33%) of the group 1, 17 (65%) of the group 2, and 8 (61%) of the group 3. Patients with no evidence of disease were more than 80% of patients in the group 1 and 2, whereas 8% in the group 3. Patients who died of their disease resulted 84% of patients in the group 3, whereas less than 5% in the group 1 and 2. Though cause-specific survival rate resulted more than 90% in the group 1 and 2 (mean follow-up 35.2 and 30.1 months, respectively), it was 15% in the group 3 (mean follow-up 30.6 months).
Table 3

Lymphoepithelioma-like carcinoma of the urinary bladder: histological subgroups according to the classification of Amin et al .

Features

Group 1- Pure

Group 2- Predominant

Group 3- Focal

Number of patients

39 (49%)

26 (34%)

13 (17%)

  Male

21

14

11

  Female

2

12

2

  NA

16

-

-

Age

   

  Mean

67.8

72.7

71.6

  Range

52-81

55-90

58-84

Stage

   

  T1

7 (18%)

1 (3%)

2 (15%)

  T2

21 (54%)

16 (62%)

7 (54%)

  T3

8 (22%)

9 (35%)

4 (31%)

  T4

2 (6%)

-

-

Primary treatment

   

  TURBT

23 (59%)

14 (54%)

7 (54%)

  Partial cystectomy

2 (5%)

2 (8%)

-

  Radical cystectomy

14 (36%)

10 (38%)

6 (46%)

Adjuvant treatment

   

  Systemic chemotherapy

15 (38%)

3 (12%)

1 (8%)

  Radiotherapy

6 (16%)

5 (19%)

3 (23%)

  Chemoradiotherapy

2 (5%)

1 (4%)

1 (8%)

  Intravesical chemotherapy

3 (8%)

-

-

  Not performed

13 (33%)

17 (65%)

8 (61%)

Follow-up

   

  Mean

35.2

30.1

30.6

  Range

2-216

2-104

0-84

Outcome

   

  Not evidence of disease (NED)

31 (81%)

20 (84%)

1 (8%)

  Died of disease (DOD)

1 (3%)

1 (4%)

11 (84%)

  Died without disease (DWD)

5 (13%)

2 (8%)

1 (8%)

  Alive with metastases (AWM)

1 (3%)

1 (4%)

-

Cause-specific survival rate

97%

95%

15%

GH Gross hematuria, TURBT Transurethral resection of the bladder tumor.

Discussion

LELCB affects primarily the elderly with male predominance, 74% of cases reported in the literature (Table 2). With respect to chief complaint, GH was observed in all available patients with presenting symptoms. Most patients with LELCB have muscle invasive T2–3 disease, regardless of histological classification (pure, predominant, and focal). In fact, as shown in Tables 2 and 3, LELCB patients with T2–3 stage resulted 83% in overall population, 76% in group 1 (pure), 97% in group 2 (predominant), and 85% in group 3 (focal). Despite its infiltrative predisposition, the metastatic potential of LELC seems to be low [1, 6]. LELCB is diagnosed at less advanced stages and has a more favorable long-term prognosis than other types of undifferentiated invasive carcinoma of the bladder.

The histological features of LELCB include an inflammatory infiltrate and a dense lymphocytic infiltrate; furthermore, the syncytial arrangement of large neoplastic epithelial cells with prominent nuclei and nucleoli can be observed [24, 25]. Once LELCB is identified, a primary tumor in the nasopharynx should be excluded with CK7 stain. Nasopharyngeal carcinomas do not express CK7. Other differential diagnosis usually includes malignant lymphoma, undifferentiated urothelial carcinoma with prominent lymphoid infiltrate, chronic cystitis, and small cell carcinoma of the bladder [1, 2, 4, 7]. These can be excluded by relevant immunohistochemistry [1, 2, 4, 8, 26].

In Table 2, a previous pooled analysis showed that at a mean follow-up of 30.4 months, 67% of the overall population did not show any evidence of disease with a cause-specific survival rate of 83%. The cause-specific survival rate was more than 90% for both pure and predominant LELCB (mean follow-up of 35.2 and 30.1 months, respectively), whereas it was 15% (mean follow-up 30.6 months) for focal LELCB. The pure and predominant subtypes are more favorable than the focal subtype in prognosis, which may be related to the inflammatory infiltrate that results in a strong immune response against the atypical cells [4], early presentation of lower urinary tract symptoms [2], and to the chemoradiosensitivity of the neoplastic cells. This prognosis may be related to the host response, seen as a dense infiltrate composed predominantly of T-lymphocytes in the tumor [4], similar to medullary carcinoma of the breast and seminoma which also contain T-lymphocytes.

To date, owing to the scarcity of reported cases, there are no clear guidelines for the treatment of LELCB whose biological behavior differs from that of conventional urothelial carcinoma. Primary treatments for LELCB include both TURBT and partial or radical cystectomy. LELCB is sensitive to both cisplatin-based chemotherapy and radiotherapy, both of which have been used as adjuvant treatments after TURBT or radical bladder surgery [1, 2, 4]. Adjuvant combination chemotherapy includes three to five courses of methotrexate, vinblastine, doxorubicin, and cisplatin [1, 2, 4, 9, 26]. As shown in Table 3, the highest mortality was detected in the patients with focal LELCB who had local radical surgery, which was not followed by any adjuvant treatment in 61% of the patients. At about the same mean follow-up as focal subtype (group 3), 84% of the patients with predominant LELCB were alive and disease free although 65% of patients did not undergo any adjuvant treatment. These findings indicate that adjuvant treatment with chemotherapy and/or radiotherapy after local treatment of the primary tumor is advised for patients presenting with focal LELCB. Bladder-preservation therapy by performing both TURBT alone or combined with adjuvant chemotherapy and/or radiotherapy may be a reasonable option for patients with pure or predominant LELCB, whereas radical surgery with adjuvant treatment may be indicated for focal LELCB with muscle invasion. In addition, because the focal LELCB patients treated with even radical surgery alone had comparatively short survival (6, 18, and 19 months) in Table 1, we thought that adjuvant treatment was essential for procedure of focal LELCB. As shown in Tables 1 and 3, most patients (84%) with focal LELCB died of the primary tumor, whereas two patients of them, who underwent radical cystectomy and adjuvant treatment, had a relatively favorable outcome (64 and 84 months in survival). The apparently more aggressive nature of focal LELCB suggests that these patients are probably best managed with radical cystectomy and adjuvant treatment.

The present case was predominantly composed of LELCB accompanied by non-invasive urothelial carcinoma. On the basis of recommendations in the published literature, the patient underwent concurrent chemoradiotherapy after TURBT, leading to bladder-preservation. Twelve months after the initial visit, no evidence of disease recurrence was observed.

Previous reports and our experience suggest that radical cystectomy may not be necessary for all patients with muscle invasive LELCB and that radiotherapy and chemotherapy may be reliable treatment options. As Kozyrakis et al. [3] also said, pathological information might be useful in selecting patients suitable for bladder-preservation treatment. However, a large-scale study with long-term follow-up is needed to better understand the biological behavior of LELCB.

Conclusion

Because LELCB is sensitive to both chemotherapy and radiotherapy, radical cystectomy may not be necessary for all patients with muscle invasive LELCB. Therefore, pathological information might be useful in selecting patients suitable for bladder-preservation treatment.

The apparently more aggressive nature of focal LELCB suggests that these patients are probably best managed with radical cystectomy and adjuvant treatment.

Consent

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.

Abbreviations

LELC: 

Lymphoepithelioma-like carcinoma

LELCB: 

LELC of the urinary bladder

WBC: 

White blood cell

MRI: 

Magnetic resonance imaging

CT: 

Computed tomography

TURBT: 

Transurethral resection of the bladder tumor

GH: 

Gross hematuria

NA: 

Not available

PU: 

Pure

PR: 

Predominant

F: 

Focal

TURBT: 

Transurethral resection of the bladder tumor

PC: 

Partial cystectomy

RC: 

Radical cystectomy

CH: 

Chemotherapy

RT: 

Radiotherapy

IV-CH: 

Intravesical chemotherapy

NED: 

Not evidence of disease

DOD: 

Died of disease

DWD: 

Died without disease

AWM: 

Alive with metastases.

Declarations

Acknowledgements

We are thankful to Dr. Mori and Dr. Mimata of the department of urology, Oita university, Japan for providing their information.

Authors’ Affiliations

(1)
Department of Urology, JA Onomichi General Hospital, Hiroshima
(2)
Department of Urology, Integrated Health Sciences, Institute of Biochemical and Health Sciences, Hiroshima University

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© Yoshino et al.; licensee BioMed Central Ltd. 2014

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