Endometriosis: A Rare Cause of Gross Hematuria

In: International Journal of Cancer Management · 2018 · vol. 11(2) · doi:10.5812/ijcm.9691 · W2790040181
article OA: diamond CC0 ⤵ 2 in-corpus citations
AI-generated summary by claude@2026-06, 2026-06-08

This case report describes a 34-year-old woman whose gross hematuria was caused by bladder endometriosis, which was treated with hormonal therapy and surgical resection.

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AI-generated deep summary by claude@2026-06, 2026-06-14 · read from full text

This paper is a case-based report discussing gross hematuria and urinary frequency due to rare mullerian pathology of the bladder, in the context of differential diagnosis with eosinophilic cystitis and urothelial carcinoma. The authors describe a posterior bladder wall mass and report management using an LH-RH analogue (selected based on a prior report), while noting that metaplasia in urothelium can be driven by chronic inflammatory or procedural stimuli and that eosinophilic cystitis was considered until pathology clarified the diagnosis. A key limitation is that the evidence is drawn from a single patient experience and literature parallels, emphasizing rarity and limited generalizability. This paper is centrally about endometriosis — specifically, it argues that endometriosis (and related non-neoplastic mullerian lesions) should be considered in patients presenting with gross hematuria.

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Abstract

Introduction: Endometriosis is a condition in which endometrial tissue exists outside the uterine cavity. Urinary tract lesions are present in 1 % of women with this condition. Case Presentation: A 34-year-old woman was presented to our clinic with a 3-year history of dysuria and frequency. Her past medical history was significant for cesarean sections, performed 3 years earlier. In our center, the patient underwent cystoscopy and transurethral resection of a lesion found in the bladder wall, which on histopathology examination appeared to be endometriosis. A course of six-month hormonal therapy with luteinizing hormone-releasing hormone (LHRH)-agonist (Dipherelin™ 3.75 IM per 28 day) was planned for her. One month later, trans-vaginal ultrasound revealed a nodule posterior to the bladder, which had grown 1 cm in the preceding month. Therefore, Hysterectomy, bilateral oophorectomy, and partial cystectomy were performed. The pathology report was Mullerianosis. During two years of follow up, the patient remained asymptomatic. Conclusions: Endometriosis and endocervicosis should be regarded as important differential diagnoses in patients with gross hematuria and those suspected to have urothelial carcinomas.
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Endometriosis is a condition described as growth of ectopically located endometrial tissue in sites other than uterine cavity. Since gross hematuria and frequency are rare symptoms of endometriosis, this diagnosis should be kept in mind in encountering these symptoms, even in the absence of other endometriosis features ( 6). Previously, mullerianosis has been indicated as the cause of microscopic hematuria in a case study, in 2012. In this study a mass intruding into the posterior aspect of the bladder was found, and for management LH-RH analogue was used, which achieved acceptable results ( 7). Therefore, we tried this treatment in managing our patient. Metaplasia (a change in cell morphology into another cell type that is considered abnormal for that location) frequently occurs in urothelium, supposedly as a response to local stimuli (e.g. urinary tract infection, inflammation especially chronic, calculi, diverticula, catheterization, or surgical procedures). Involvement of genitourinary tract with one of the non-neoplastic mullerian lesions includes: endocervicosis, endometriosis or endosalpingiosis occurs in 1 to 2% of cases, most of which are endometriosis ( 2). Conversely, endocervicosis is considered a rare condition, which was first described as a distinct concept, by Clement and Young in 1992, as a benign variation of endometriosis ( 8). Ever since, few cases of this entity occurring almost exclusively in women of reproductive age have been reported. This condition is characterized by existence of mucinous endocervical epithelium within the detrusor muscle of the bladder ( 9). This situation is characterized by the following features: occurring during reproductive age, being located in the posterior bladder wall and coexisting with endometriosis and endosalpingiosis ( 10). Among different predisposing factors associated with endocervicosis, history of previous Caesarean section appears to be the most prominent one ( 11). This association is not only apparent from our report, but it also is shown by all previous cases reported in this regard ( 12). They all have the same presentations as our case, with the main clinical features including a mass in the bladder and urinary complaints. Although this condition is very rare, considering the features of our case, it should be envisaged as a possible diagnosis. Eosinophilic cystitis, an uncommon inflammatory bladder condition, for which the pathophysiology is still unknown, usually presents with hematuria, frequency, urgency and supra-pubic pain, in addition to sterile urine culture ( 13). Since we had two of these symptoms in our case this condition was considered a differential diagnosis until the pathology reported otherwise. There are different causes for hematuria ranging from benign to malignant yet endometriosis and endocervicosis should be regarded in patients with gross hematuria and in differential diagnosis of urothelial carcinoma.

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last seen: 2026-06-10T17:14:06.276822+00:00
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