scholarly journals Primary hydatid cyst of the urinary bladder

2018 ◽  
pp. bcr-2018-226341 ◽  
Author(s):  
Sardar Hassan Arif ◽  
Ayad Ahmad Mohammed
Keyword(s):  
Abdominal Pain ◽  
Urinary Bladder ◽  
Hydatid Cyst ◽  
Lower Abdominal Pain ◽  
Complete Excision ◽  
Abdominal Tenderness ◽  
Superior Part ◽  
Rim Enhancement ◽  
Abdominal Examination ◽  
Primary Hydatid Cyst

A 35-year-old man presented with poorly localised lower abdominal pain for 3 months. Abdominal examination revealed lower abdominal tenderness, with normal other parts of examination. CT scan of the abdomen showed irregular multiloculated mass related to the upper part of the urinary bladder with mild rim enhancement in the postcontrast study with no areas of calcifications. During laparotomy, we found a mass attached to the superior part of the urinary bladder and arising from its wall. Complete excision was done without opening the cavity of the bladder. The mass was opened and was a hydatid cyst of the bladder containing multiple daughter cysts.

scholarly journals Hydatidosis of the Pelvic Cavity: A Big Masquerade

2008 ◽  
Vol 2008 ◽  
pp. 1-3 ◽  
Author(s):  
Peyman Varedi ◽  
Seyed Reza Saadat Mostafavi ◽  
Rambod Salouti ◽  
Daryoush Saedi ◽  
Seyed Ali Nabavizadeh ◽  
...  
Keyword(s):  
Weight Loss ◽  
Differential Diagnosis ◽  
Abdominal Pain ◽  
Hydatid Cyst ◽  
Unusual Presentation ◽  
Pelvic Cavity ◽  
Surgical Exploration ◽  
Pelvic Masses ◽  
Microscopic Studies ◽  
Primary Hydatid Cyst

We report and discuss a case of primary hydatidosis of the pelvic cavity in a woman who presented with severe weight loss and abdominal pain. This unusual presentation was initially considered as a tumor process until surgical exploration and microscopic studies confirmed the diagnosis. The gynecologists should be aware of possibility of primary hydatid cyst of the pelvic cavity and should be considered in the differential diagnosis of cystic pelvic masses, especially in areas where the disease is endemic.

scholarly journals Procidencia with rare complication -a case report

KYAMC Journal ◽  
2013 ◽  
Vol 3 (1) ◽  
pp. 262-264
Author(s):  
Mst Atia Sultana ◽  
Monira Akter ◽  
Shafiul Anam
Keyword(s):  
Abdominal Pain ◽  
Case Report ◽  
Rare Complication ◽  
Lower Abdominal Pain ◽  
Chemical Substances ◽  
Abdominal Tenderness ◽  
History Of

Mrs. Lalbanu 65 years old lady presented to us with the complaints of something coming down per vagina for 10 years, foul smelling discharge for 2 months, fever & maggot formation for 5 days, she  also gave history of applying some chemical substances on her prolapsed mass of genitalia, and she also complains of lower abdominal pain for last 5 days. On examination, prolapsed mass was distorted, edematous, infected, irreducible & there were maggots, her temperature was raised & having lower abdominal tenderness. She was treated at first conservatively & then surgically. Now  she is well & with our follow up.DOI: http://dx.doi.org/10.3329/kyamcj.v3i1.13662 KYAMC Journal Vol. 3, No.-1, June 2012 pp.262-264

scholarly journals Pelvic Hydatid Cyst with Hydroureteronephrosis: A Rare Case Report

2021 ◽  
Vol 2021 ◽  
pp. 1-4
Author(s):  
Amir Mohammad Salehi ◽  
Hossain Salehi ◽  
Ensiyeh Jenabi
Keyword(s):  
Abdominal Pain ◽  
Case Report ◽  
Hydatid Cyst ◽  
Rare Case ◽  
Parasitic Disease ◽  
Body Parts ◽  
Antibody Index ◽  
Rare Case Report ◽  
Primary Hydatid Cyst ◽  
Cystic Masses

Hydatid cyst is a parasitic disease caused by Echinococcus granulosus or Echinococcus multilocularis. Humans are accidentally infected with the parasite. The cyst is usually found in the liver and lungs and rarely occurs in other body parts. The present article describes a rare case of pelvic hydatid cyst in a young man who presented with nausea, vomiting, and right abdominal pain. Two large cystic masses were discovered during a CT scan in the patient’s pelvic region, resulting in right urinary tract hydroureteronephrosis. Additionally, the antibody index was used to confirm the presence of a primary hydatid cyst.

scholarly journals Inflammatory Myofibroblastic Tumor of the Urinary Bladder with Atypical Clinical and Pathological Features: a Case Report

2021 ◽  
Author(s):  
Zhu Xingwang ◽  
Wang Yixiang ◽  
Liu Yili
Keyword(s):  
Abdominal Pain ◽  
Urinary Bladder ◽  
Clinical Features ◽  
Inflammatory Myofibroblastic Tumor ◽  
Lower Abdominal Pain ◽  
Partial Cystectomy ◽  
Ki 67 ◽  
Case Presentation ◽  
Anaplastic Lymphoma ◽  
Bladder Dome

Abstract Background: The inflammatory myofibroblastic tumor (IMT) of urinary bladder is very rare, this case and often misdiagnosed as bladder cancer. We report a patient with atypical clinical features with dysuria and lower abdominal pain. Case presentation: A 32-year-old man presented with dysuria and lower abdominal pain. Computed tomography (CT) demonstrated that a solitary non-papillary tumor was located at the wall of the bladder dome. Partial cystectomy was successfully managed. Immunohistochemically, positivity of the tumor cells for anaplastic lymphoma kinase (ALK), Actin (SM), vimentin, cytokine (CK), epithelial membrane antigen (EMA) and Ki-67. Based on the the above clinical features、histopathology and immunohistochemical, the tumor was definitively diagnosed as bladder’s IMT. After 24 months, there was no signs of recurrence and metastasis with CT and cystoscopy.Conclusion: A rare case of inflammatory myofibroblastic tumor of urinary bladder after partial cystectomy was reported. It is essential for urologists and scientists to entirely understand the characteristics of the inflammatory myofibroblastic tumor and make a better clinical guideline, to avoid over treatments.

scholarly journals Spontaneous Rupture of Urinary Bladder (SRUB) in a Young Male, Presenting as Anuria – A Case Report and Review of Literature

2014 ◽  
Vol 7 (1) ◽  
pp. 64-66
Author(s):  
Sekar Hariharasudhan ◽  
Sriram Krishnamoorthy ◽  
Sunil Shroff
Keyword(s):  
Abdominal Pain ◽  
Case Report ◽  
Urinary Bladder ◽  
Spontaneous Rupture ◽  
Lower Abdominal Pain ◽  
Young Male ◽  
Bladder Rupture ◽  
Emergency Laparotomy ◽  
High Morbidity ◽  
Delay In Diagnosis

Spontaneous rupture of urinary bladder is a rare condition. Most of the bladder ruptures occur in association with blunt or penetrating injuries to the lower abdomen. Most often, a vague lower abdominal pain is the mode of presentation. Rarely patients present with oliguria, anuria, uremia or urosepsis. A forty year old male, under the influence of alcohol, presented with lower abdominal pain and anuria for two days with abnormal renal function. He denied history of blunt trauma. He was diagnosed to have an intra-peritoneal rupture of urinary bladder. He underwent emergency laparotomy with repair of bladder rupture. This case report illustrates the need for a high index of clinical suspicion. Prompt diagnosis and appropriate management will help in preventing a poor clinical outcome in patients with spontaneous bladder perforation. If left untreated or if there is a considerable delay in diagnosis and intervention, it usually is associated with a high morbidity.

scholarly journals ISOLATED PRIMARY HYDATID CYST OF THE PANCREAS: A CASE REPORT

2015 ◽  
Vol 8 (1) ◽  
Author(s):  
Mehmet Eren Yuksel ◽  
Bulent Aytac ◽  
Ahmet Karamercan
Keyword(s):  
Abdominal Pain ◽  
Hydatid Cyst ◽  
Surgical Intervention ◽  
Treatment Options ◽  
Abdominal Ultrasound ◽  
The Body ◽  
Stage 4 ◽  
Primary Hydatid Cyst ◽  
Caucasian Female ◽  
Vague Abdominal Pain

Hydatid disease is caused by tapeworm Echinococcus granulosus. E. granulosus forms hydatid cysts in human body, mostly in the liver and the lung. However, isolated primary hydatid cyst of the pancreas is rarely seen. Hereby, we report a 40-year-old Caucasian female with a hydatid cyst in the body of the pancreas. The patient, complaining of vague abdominal pain was examined with abdominal ultrasound. The ultrasound scan of abdomen revealed an exophytic cystic lesion in the body of the pancreas, approximately 7.5x5 cm in size. The defined lesion was thought to be compatible with hydatid cyst stage 4-5. The  surgical team informed the patient about all possible treatment options. The patient was put on albendazole treatment, 400 mg twice daily, for two months. Despite the medical treatment, the patient complained about abdominal pain and discomfort affecting her daily life. Therefore, she decided for surgical intervention. Following the intraoperative application of scolicidal hypertonic 20% NaCl solution, partial cystectomy with capitonnage was performed. The patient did well postoperatively. Isolated primary hydatid cyst of the pancreas is rarely seen, however, it should be taken into account in the differential diagnosis of abdominal pain, especially in endemic areas. 

scholarly journals Abdominopelvic Actinomycosis Mimicking Peritoneal Carcinomatosis: A Case Report

2020 ◽  
Vol 36 (6) ◽  
pp. 417-420
Author(s):  
Sungjin Kim ◽  
Sung Il Kang ◽  
Sohyun Kim ◽  
Min Hye Jang ◽  
Jae Hwang Kim
Keyword(s):  
Abdominal Pain ◽  
Case Report ◽  
Peritoneal Carcinomatosis ◽  
Histopathological Examination ◽  
Lower Abdominal Pain ◽  
Preoperative Imaging ◽  
Imaging Studies ◽  
Complete Excision ◽  
Pelvic Masses ◽  
History Of

Actinomycosis is a rare chronic bacterial infection primarily caused by <i>Actinomyces israelii</i>. A 47-year-old woman presented to our clinic with a 1-week history of lower abdominal pain. Preoperative imaging studies revealed multiple peritoneal and pelvic masses suggestive of malignancy. The primary tumor could not be identified despite further endoscopic and gynecological evaluation. On exploration for tissue confirmation, excisional biopsies from multiple masses were performed because complete excision was not possible. Histopathological examination confirmed actinomycosis with multiple abscesses, and the patient was treated with antibiotics. We present a case of disseminated peritoneal actinomycosis that mimicked malignant peritoneal carcinomatosis on imaging studies.

scholarly journals OHVIRA syndrome with Orofacial clefts: a rare association

2020 ◽  
Vol 9 (3) ◽  
pp. 1306
Author(s):  
Sambedna . ◽  
Amit Kumar ◽  
Mukta Agarwal ◽  
Nimisha Agrawal ◽  
Sudwita Sinha
Keyword(s):  
Abdominal Pain ◽  
Iliac Fossa ◽  
Left Kidney ◽  
Lower Abdominal Pain ◽  
Left Iliac Fossa ◽  
Renal Anomaly ◽  
Tender Mass ◽  
Abdominal Examination ◽  
Ohvira Syndrome ◽  
Obstructed Hemivagina

Obstucted hemivagina with ipsilateral renal anomaly (OHVIRA) syndrome or Herlyn-Werner-Wunderlich syndrome (HWW) is a rare congenital anomaly consist of uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis. We are reporting an adolescent girl with orofacial defect who presented with lower abdominal pain. She attained menarche 3 months earlier and had a regular menstrual cycle with cyclical abdominal pain. On abdominal examination a firm, mobile tender mass extending from left iliac fossa up to umbilicus (24 weeks size) was found.  Lower border of mass could not be approached. Further evaluation with ultrasound showed enlarged uterus with collection with internal echoes and non-visualization of the left kidney. CECT showed absent left kidney and didelphys uterus with large left hematocolpometra with left complex adenexal cyst. Patient was posted for hematocolpos drainage and vaginoplasty. An unusual presentation of regular menstruation and nonspecific abdominal pain delays the diagnosis, which can lead to severe complications such as endometriosis and infertility.

scholarly journals Back bugged: A case of sacral hydatid cyst

2010 ◽  
Vol 01 (01) ◽  
pp. 43-45 ◽  
Author(s):  
Dipak Patel ◽  
Dhaval Shukla
Keyword(s):  
Back Pain ◽  
Hydatid Cyst ◽  
Spinal Canal ◽  
Cystic Lesion ◽  
Bone Erosion ◽  
Complete Excision ◽  
Primary Hydatid Cyst ◽  
Magnetic Resonance Imaging Mri ◽  
The Right

ABSTRACTHydatid cyst of bone constitutes only 0.5 - 2% of all hydatidoses. The thoracic spine is the most common site of spinal hydatidoses. Primary hydatid cyst of the sacral spinal canal is rare. A 23-year-old gentleman had back pain fi ve years ago. At that time he was evaluated and found to have a small cyst in S1 spinal canal, which was presumed to be a benign Tarlov’s cyst; and no treatment was off ered. He continued to have back pain and also developed sciatica on the right side. Neurological examination presently revealed right S1 radiculopathy. Magnetic resonance imaging (MRI) showed a large multiloculated cystic lesion extending from L5 to S2 spinal canal with bone erosion, both anteriorly and posteriorly. He underwent L5 to S2 laminectomy and excision of multiple cysts. The whole cyst was excised and cavity irrigated with sterilized formalin. A laparoscope was introduced in the cavity to look for extension into the pelvis and to confirm complete excision. Postoperatively, the patient received albendazole for two months. At 16 months follow-up the patient was asymptomatic. Hydatid cyst of sacrum is rare and can be missed at initial presentation. If the patient with a cystic lesion of sacral continues to have symptoms the diagnosis should be revaluated and prompt treatment should be off ered.

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