Tag Archive for: Hematuria



In urological practice, bladder perforations are often seen in the context of trauma or as a complication of surgery. Here we report the second case of bladder perforation caused by a large pelvic hematoma without direct injury to the bladder.The patient was a 46-year-old woman. She was admitted to the hospital with cardiogenic shock. One week after a percutaneous coronary angiography performed through the right femoral artery, she presented with gross hematuria. A CT scan of her abdomen and pelvis revealed a large right pelvic hematoma compressing the bladder and producing bilateral hydronephrosis. A suspected extraperitoneal perforation of the right bladder wall was later confirmed by cystoscopy and cystography. Although conservative management is the standard recommendation for extraperitoneal bladder perforations, we performed a combined transvesical/extravesical primary open repair in two layers, as conservative management failed in the only similar case that had been previously reported in the literature.

Authors: Marchant, Fernando; Ossandón, Enrique; Fleck, Daniela; Sepúlveda, Francisco; Mercado, Alejandro

Corresponding Author: Alejandro Mercado. University of Chile Clinical Hospital. Department of Urology. Avenida Santos Dumont 999, Piso 5 Sector A. Independencia, Santiago, Chile. Phone: +5629788503. E-mail: [email protected]

In urological practice, bladder perforations are often seen in the context of trauma or as a complication of surgery1. Here we report the second case of bladder perforation caused by a large pelvic hematoma without direct injury to the bladder, resulting in gross hematuria.

Case report

A 46-year-old woman with history of obesity, diabetes mellitus and chronic arterial hypertension presented to her local hospital with progressive dyspnea. Initial evaluation with a chest x-ray revealed bilateral pleural effusion and basal consolidation in the right lung. She developed respiratory, renal and heart failure, requiring management in an intensive care unit. Emergency percutaneous coronary angiography performed through the right femoral artery ruled out any coronary lesions, but the ventriculography revealed a dilated cardiopathy with an ejection fraction of 25%. After stabilization she was transferred to the intensive cardiology unit of our institution for further management. One week after the coronary angiography, a urologican consultation was requested as the patient developed gross hematuria. On physical examination she had a normal blood pressure and heart rate, her abdomen was soft and non tender, with no palpable masses, bruises or visible hematoma. In the right groin she had the scar from the percutaneous access for coronary angiography, with no sign of any complications. An urinary catheter was in place, with gross hematuria and abundant clots in the urine collection bag. A gentle bladder wash was performed, producing several clots, but not being able to recover clear urine. A three-way urinary catheter with continuous saline irrigation was left in place and an abdominal and pelvis CT scan was requested. The images revealed a large right pelvic hematoma of 15 x 9 cm compressing and deviating the bladder to the left, with secondary moderate bilateral hydronephrosis (Fig. 1). Active bleeding was ruled out with CT angiography. An extraperitoneal perforation of 2 x 3 cm at the right bladder wall was suspected and later confirmed by cystoscopy and cystography (Fig. 2). The case was discussed at the clinical meeting of the urology department. Based on the failure of conservative management reported in the only similar case published in the literature by Lane et al. (2004) (2), we attempted a primary open repair. A midline infraumbilical abdomen incision was used to access the Retzius space. A longitudinal anterior cystotomy was performed and the perforation was identified at the right bladder wall, close to the trigone area where the balloon of the urethral catheter rested. As the perforation was difficult to reach transvesically, we decided to change to a combined intravesical/extravesical approach, for which it was necessary to free the right bladder wall from, and remove, the pelvic hematoma (Fig. 3). The borders of the perforation were resected and the repair was performed in two layers. A suprapubic catheter and a perivesical drain were left in place upon closure of the bladder and abdomen. The patient did not develop any postoperative complications and was discharged a week after. Cystography performed 3 weeks after surgery showed integrity of the bladder with no extravasation of contrast medium (Fig. 4). The cystostomy catheter was removed after 4 weeks and to the date the patient is voiding normally and is free of any bladder-related symptoms.

Gross hematuria in hospitalized patients can be explained by several medical conditions. Generally is related to traumatic catheterization or instrumentation. Other causes include urinary tract infections, bladder or renal tumors, blood dyscrasias and chemotherapy (2). Here we report the second case of bladder perforation produced by a large pelvic hematoma resulting in hematuria. The first case was reported by Lane et al. (2004) (2).
The recommended standard treatment of uncomplicated extraperitoneal bladder perforations, when conditions are ideal, is conservative management with catheter drainage alone (1). However, some authors (3,4) have reported fewer complications, such as fistula, failure to heal, clot retention, and sepsis, with open repair (5% overall) versus conservative management (12% overall). For this reason, extraperitoneal perforations with any complicating features should be managed with primary open repair to prevent complications.
The similarity of this case to the one reported by Lane et al. (2004) (2) is impressive. Both patients had a percutaneous coronary angiography with access through the right femoral artery. In both cases the pelvic hematoma was on the right side, correlating to the site of arterial puncture. In both cases the perforation occurred close to the bladder neck, in the right bladder wall. We agree with Lane et al. (2004) (2) in that the most likely cause of bladder perforation was pressure necrosis that developed between the hematoma and the balloon of the Foley catheter. Considering the failure of conservative management reported in the case of Lane et al. (2004)(2), we aimed to attempt a primary open repair for two reasons: first, as the perforation occurred at the site where the balloon of the catheter rests, the same balloon could prevent the closure of the wound; second, leaving this patient with a communication between the bladder and hematoma, and with an indwelling catheter, carried a high risk of complications, as infection could easily lead to cardiovascular decompensation in this particular patient.
This report supports pelvic hematomas as cause of bladder perforation, probably secondary to compression of the bladder wall against the balloon of a Foley catheter. Here we also suggest that in this kind of extraperitoneal bladder perforations, primary open repair could be a better option than conservative management.

077Figure 1














Figure 1 Pelvis CT scan. Large (9 x 15 cm) right pelvic hematoma (*) compressing the bladder (B). The arrow points the site of perforation, in direct relation to the balloon of the Foley catheter (f).

077Figure 2














Figure 2 Preoperative cystography. Retroperitoneal extravasation (E) of contrast from the bladder (B), which is deviated to the left by the pelvic hematoma.

077Figure 3














Figure 3 Postoperative cystography (3 weeks after surgery). No contrast extravasation was observed from the bladder (B), now on a central position. Cystography was performed through the suprapubic catheter.

1. Morey AF, Rozanski TA. Bladder Injuries. In Wein AJ, Kavoussi LR, Novick AC, Partin AW, Peters CA. (Editors): Campbell-Walsh Urology, 9th Edition. Philadelphia, WB Saunders, 2007, vol 3, 2655-2658.
2. Lane BR, Moy L, Frenkl T, Hijaz A, Daneshgari F. Pelvic hematomas as a cause of bladder perforation and gross hematuria. Urology 2004; 64: 1030.e7-1030.e8.
3. Cass AS. Diagnostic studies in bladder rupture. Urol Clin North Am 1989; 16: 267-273.
4. Kotkin L, Koch MO. Morbidity associated with nonoperative management of extraperitoneal bladder injuries. J Trauma 1995; 38: 895-898.


Date added to bjui.org: 13/12/2012

DOI: 10.1002/BJUIw-2012-077-web


Metastatic Papillary Thyroid Carcinoma to the Prostatic Urethra Presenting as Gross Hematuria

Papillary thyroid cancer (PTC) is the most common welldifferentiated cancer of the thyroid. While regional metastatic disease to lymph nodes is most common, there have been rare cases of distant metastases to the kidney. We report a case of papillary thyroid carcinoma (PTC) with metastases to the prostatic urethra presenting as gross hematuria.

Authors: Vora, Anup; Krishnan, Jayshree; Verghese, Mohan

Corresponding Author: Vora, Anup


Case Report
A 31-year-old Indian male with a known history of metastatic papillary thyroid cancer was referred for investigation of intermittent gross haematuria. The patient was first diagnosed with PTC at age 4 and was treated with subtotal thyroidectomy, followed by radioactive iodine (I-31) therapy. The patient underwent a second course of radioactive I-31 therapy several years later for metastatic disease to the lungs and eventually underwent a total thyroidectomy in 2007. He received a third course of I-31 infusion in 2009 followed by trial of sunitinib for disease unresponsive to radioactive Iodine therapy. Radiographic imaging revealed a 1.9 cm enhancing mass in the interpolar region of the right kidney .Microscopic examination of the kidney biopsy showed focal infiltration by cohesive malignant cells including a papillary cluster, with the cells showing nuclear grooves. Immunohistochemical stains showed that the tumour cells were positive for thyroglobulin and thyroid transcription factor-1 (Figure 1).
With regards to haematuria, the patient denied any previous significant genitourinary history. Haematuria was intermittent and painless with passage of small clots. The patient was taken to the operating room and underwent diagnostic cystoscopic evaluation of his lower urinary tract. Cystoscopy revealed friable frond-like tissue in the prostatic urethra, with mucosal sloughing and bleeding. Bladder urothelium was grossly normal, with bilateral efflux of clear urine from the ureteral orifices. Microscopic examination of the tissue showed sheets of tumour cells with nuclear crowding, nuclear grooves and intranuclear inclusions. Immunostains showed that the tumour cells are positive for thyroid transcription factor 1 and thyroglobulin (Figure 2). Urine cytology and cell block also showed similar tumour cells.
Histomorphological features and the immunohistochemical staining features in both the renal and prostatic urethral tumor tissue supported a diagnosis of metastatic thyroid carcinoma.

Although the prognosis of PTC is generally good, up to 10% of the patients eventually die of the disease and greater proportion would face the morbidity of recurrences. PTC is known to metastasize preferentially to lymph nodes, and distant metastases may be present in upto 10% of patients during the course of follow-up. [1] The most common metastatic locations include the lungs, bones and brain.However, rare cases of metastatic PTC have been reported in the scalp [2], pancreas [3] and maxilla [4]. A small number of metastastic renal lesions have been reported [5]. These cases typically occured after a long latency period followingprimary therapy. There have been no known reported cases of metastatic deposits in the prostatic urethra [1,6]. Other malignancies that have reported metastases to the urethra include rectal adenocarcinoma [7] and malignant melanoma [8].
In the management of patients who have distant PTC metastases, lesions in areas where continued growth into surrounding structures would result in serious morbidity should be addressed with surgical or other palliating treatment. Lesions in the brain, spinal column, weight-bearing bones, or upper mediastinum could progress and result in acute spinal cord compression, superior vena cava syndrome or an acute central nervous system event from brain metastases [6].
We present a rare case of metastatic PTC to the prostatic urethra resulting in intermittent, painless gross haematuria. Fulguration of the lesion resulted in a short term control of bleeding only. Our patient is currently considering external beam radiotherapy to the prostatic urethra to palliate his gross haematuria and further systemic therapy for diffuse metastatic disease.


Figure 1: Microscopic examination of the kidney biopsy showed focal infiltration by cohesive malignant cells including a papillary cluster, with the cells showing nuclear grooves (A/B haematoxylin& eosin stain with magnification x 25). Immunohistochemical stains showed that the tumour cells were positive for thyroglobulin and thyroid transcription factor-1(C) . D. Immunostain for thyroglobulin, magnification x 40.


Figure 2. Microscopic examination of this prostatic urethral biopsy tissue showed sheets of tumour cells with nuclear crowding, nuclear grooves and intranuclear inclusions (A. magnification x 25, B. magnification x 40. Immunostains showed that the tumour cells are positive for thyroid transcription factor 1 (C. magnification x 25) and thyroglobulin (D. magnification x 40).

1. Pakdaman MN, Rochon L, Gologan O et al. Incidence and histopathological behavior of papillary microcarcinomas: Study of 429 cases. Otolaryngol Head Neck Surg2008;139:718–22.

2. Aghasi MR, Valizadeh N, Soltani S. A 64 year-old female with scalp metastasis of papillary thyroid cancer.Indian J EndocrinolMetab. 2011 Jul;15:136-7.

3. Borschitz T, Eichhorn W, Fottner C et al. Diagnosis and treatment of pancreatic metastases of a papillarythyroid carcinoma. Thyroid. 2010 Jan;20(1):93-8.

4. Nikitakis NG, Polymeri A, Polymeris A, Sklavounou A. MetastaticPapillaryThyroid Carcinoma to the Maxilla: Case Report and Literature Review. Head Neck Pathol.2011 Dec 30.epub

5. Borde C, Basu S, Kand P, Arya S, Shet T. Bilateral renal metastases from papillarythyroid carcinoma on post 131I treatment scan: flip-flop sign, radioiodine SPET, 18F-FDG PET, CECT and histopathological correlation. Hell J Nucl Med. 2011 Jan-Apr;14(1):72-3.

6. Woolner LB, Lemmon ML, Beahrs OH, Black BM, Keating FR Jr. Occult papillary carcinoma of the thyroid gland: A study of 140 cases observed in a 30-year period. J ClinEndocrinolMetab 1960;20:89-105

7. Wakahara T, Yamamoto S, Fujita S, Akasu T, Onouchi S, Moriya Y. A case of advanced rectaladenocarcinoid tumor with long-term survival.Jpn J ClinOncol. 2010 Jul;40(7):690-3.

8. MartíMestre J, OlivaEncina J, Sánchez Martín F et al. Melanomametastatic to the female urethra. Report of a case.ActasUrol Esp. 2002 Mar;26(3):231-4.


Date added to bjui.org: 15/10/2012

DOI: 10.1002/BJUIw-2012-001-web


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