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1.
Can J Surg ; 53(1): E3-4, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20100402

ABSTRACT

Paragangliomas are extra-adrenal chromaffin tumours that develop at the expense of neuroectodermal cells of the autonomous nervous system. Retroperitoneal and nonfunctioning forms are very rare. They are often asymptomatic and can reach a substantial size. Treatment usually involves surgery with the goal of total excision. We report the case of a patient who presented with indistinct abdominal pain. This case demonstrates how the diagnosis of retroperitoneal nonfunctioning paragangliomas relies mostly on histological results.


Subject(s)
Paraganglioma/diagnosis , Retroperitoneal Neoplasms/diagnosis , Abdominal Pain/etiology , Female , Humans , Middle Aged , Paraganglioma/complications , Paraganglioma/surgery , Retroperitoneal Neoplasms/complications , Retroperitoneal Neoplasms/surgery
2.
J Med Case Rep ; 11(1): 159, 2017 Jun 16.
Article in English | MEDLINE | ID: mdl-28619080

ABSTRACT

BACKGROUND: Hepatic cystadenoma is a rare benign cystic tumor; it tends to recur after incomplete surgical resection and has malignant potential. We report the case of a patient with a ruptured biliary cystadenoma in the common bile duct that caused diagnostic and therapeutic problems. CASE PRESENTATION: A 34-year-old North African woman, admitted for angiocholitis, was operated 2 months before for a hepatic cystic lesion taken for a hydatid cyst compressing her common bile duct. The clinical and the complementary examinations converged toward recurrence of the hydatid cyst for which a surgical resection was decided. Intraoperative findings as well as the histological study of the "membranes" extracted from her common bile duct indicated a hepatic cystadenoma. CONCLUSIONS: The rarity of hepatic cystadenoma and the non-specificity of clinical and imaging signs make diagnosis of hepatic cystadenoma difficult, especially when it is complicated by rupture in the bile ducts; this contributes to a delay in diagnosis and an inadequate therapeutic approach.


Subject(s)
Bile Duct Neoplasms/diagnosis , Bile Ducts/pathology , Cystadenoma/diagnosis , Rupture, Spontaneous/pathology , Rupture, Spontaneous/surgery , Adult , Bile Duct Neoplasms/pathology , Bile Duct Neoplasms/surgery , Bile Ducts/diagnostic imaging , Cholangiography , Cystadenoma/diagnostic imaging , Cystadenoma/pathology , Cystadenoma/surgery , Female , Humans , Jaundice, Obstructive/diagnosis , Jaundice, Obstructive/etiology , Jaundice, Obstructive/pathology , Jaundice, Obstructive/surgery , Rare Diseases , Rupture, Spontaneous/diagnostic imaging , Tomography, X-Ray Computed , Treatment Outcome
3.
Pan Afr Med J ; 24: 79, 2016.
Article in French | MEDLINE | ID: mdl-27642418

ABSTRACT

Wall endometriosis is a rare clinical entity whose pathophysiology remains unclear. It occurs most frequently after gynecologic or obstetric surgery. We report the case of a patient with cyclic pain at the caesarean section scar. Clinical examination showed a 5 cm mass in the right iliac fossa. Tomodensitometry revealed a tissue density mass (45mm on the major axis). Hence, the decision to perform a wide excision of the lesion. Anatomo-pathological examination confirmed the diagnosis of parietal endometriosis. Postoperative sequelae were simple with a follow-up period of 20 months with no recurrence of the mass or of the pain. Our study highlights the characteristics of this disease to allow the health practitioner to understand the importance of diagnosis, of early treatment of this disease as well as of the possibility to prevent it during each gynecologic or obstetric surgery.


Subject(s)
Abdominal Pain/etiology , Abdominal Wall/diagnostic imaging , Cicatrix/diagnostic imaging , Endometriosis/diagnostic imaging , Abdominal Wall/pathology , Adult , Cesarean Section/adverse effects , Cicatrix/pathology , Endometriosis/pathology , Endometriosis/surgery , Female , Follow-Up Studies , Humans , Pregnancy , Recurrence , Tomography, X-Ray Computed/methods
7.
Am J Surg ; 199(2): e25-6, 2010 Feb.
Article in English | MEDLINE | ID: mdl-19954768

ABSTRACT

Retroperitoneal contamination may occur during the natural history of hydatid disease. Primary hydatid cyst of the retroperitoneum is extremely rare. The authors report a case of a giant retroperitoneal hydatid cyst. Clinicians and surgeons must be aware of this possibility and follow a policy of nonsystematic puncture of an abdominal cyst and avoid spillage during surgery. Symptoms are related to the size, location, or ensuing complications of a cyst. Its occurrence should be strongly suspected ahead of any abdominal cyst, especially in an endemic area, where it may act as a parasite. Total and careful surgical excision is the gold-standard therapy.


Subject(s)
Echinococcosis , Retroperitoneal Space , Abdominal Neoplasms/diagnosis , Agriculture , Diagnosis, Differential , Echinococcosis/diagnosis , Echinococcosis/diagnostic imaging , Echinococcosis/surgery , Humans , Male , Middle Aged , Tomography, X-Ray Computed
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