Chronic Non-Puerperal Uterine Inversion; Fibromyoma Uteri as a Cause- A Case Report
Journal Title: Scholars Journal of Medical Case Reports - Year 2014, Vol 2, Issue 2
Abstract
Non-puerperal inversion of the uterus is a rare clinical problem. Mostly diagnosis is difficult in gynecological cases. In majority of cases fundal fibroid causing inversion is the cause. Treatment depends on the associated pathology and type of the inversion. Here we report a rare case of non-puerperal uterine inversion caused by a large fundal leiomyoma in a 45 year old woman causing heavy vaginal bleeding and urinary retention. In such cases abdominal hysterectomy must be the choice as it is necessary to locate the distal urinary collecting system. Keywords: Fibroid, non‑puerperal uterine inversion, hysterectomy.
Authors and Affiliations
Jain Sapna, Aherwar Rupa, Joshi Prajakta
Giant Fibromatosis of the Chest Wall: A Rare Entity
Fibromatosis also termed as desmoids is a rare benign but locally aggressive neoplasm characterized by mass like or infiltrative growth of fibrous tissue. It usually arises from the abdominal wall or the extremities, rar...
Demographic Study of Gastrointestinal Stromal Tumors in Malaysia – A Comparison between East and West
Gastrointestinal stromal tumours (GISTs) are the commonest mesenchymal tumors of the gastrointestinal tract. We aim to compare the differences in epidemiology, presentation and tumor characteristics of GISTs in the geogr...
Spermatocytic Seminoma: A Rare Testicular Tumor
Spermatocytic Seminoma is a rare testicular tumor which has dictinct clinical presentation, histological and immunochemical features than classical seminoma and also has good prognosis. It represents 1-4% of all seminoma...
Nephrogenic adenoma of urinary bladder following intravesical BCG therapy
Nephrogenic adenoma is a rare benign disease in the urinary tract most frequently in the urinary bladder. Though the etiology is still not established but its association with trauma, urinary tract infection, stone disea...
Allgrove Syndrome: Report of Two Cases
Abstract: Allgrove syndrome or Triple A syndrome is a rare autosomal recessive disorder. The mutation affects the AAAS gene localized on chromosome 12. It combines alacrima, achalasia and adrenal insufficiency. Neurologi...