abdominal cyst
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2022 ◽  
Vol 15 (1) ◽  
pp. e245767
Author(s):  
Damini Saxena ◽  
Robert A Duncan ◽  
Robert R Faust ◽  
Anthony Campagna

Differential diagnosis of a new abdominal mass is broad and includes infection, malignancy and other inflammatory processes. Definitive diagnosis may be challenging without invasive biopsy, as history, physical exam and imaging may be non-specific. A 69-year-old man with a history of abdominal tuberculosis presented with a new painful abdominal cyst consistent with reactivation of tuberculosis versus new malignancy. Investigations revealed 4+ acid-fast bacilli from the aspirate suggestive of tuberculosis, but no improvement was noted on antituberculous therapy. Core needle biopsy noted c-KIT-positive spindle cells, diagnostic for a gastrointestinal stromal tumour, while cultures grew non-tuberculous mycobacteria.


2021 ◽  
Vol 58 (S1) ◽  
pp. 138-138
Author(s):  
T. Fanelli ◽  
N. Volpe ◽  
V. De Robertis ◽  
G. Rembouskos ◽  
A. Di Tonto ◽  
...  

2021 ◽  
Vol 5 (7) ◽  
pp. 1-1
Author(s):  
Murat BAŞARANOĞLU ◽  
Serap KARAMAN ◽  
Veli AVCİ ◽  
Kemal AYENGİN ◽  
Erbil KARAMAN

2021 ◽  
Vol 2021 (4) ◽  
Author(s):  
Venkiteswaran Muralidhar

ABSTRACT This is a report of a rare case of an infarcted pelvic intra-abdominal cyst, having no mesenteric connection presenting as an acute abdomen. The patient had significant asbestos exposure. The cyst was treated successfully by surgical excision. Histopathology showed an infarcted cyst; the lining was destroyed, precluding marker studies. A diagnosis of benign cystic peritoneal mesothelioma (BCPM) was made by excluding other causes of solitary pelvic intra-abdominal cysts. BCPM has been classified as an asbestos-related neoplasm and is usually seen in the pelvis adjunct to the urinary bladder. One-year post-surgery, there was no recurrence. The case report shows that infarcted pelvic mesothelial cysts can present as an acute abdomen and can be treated successfully by total excision with no recurrence.


Medicina ◽  
2020 ◽  
Vol 56 (11) ◽  
pp. 583
Author(s):  
Liana Ples ◽  
Radu Chicea ◽  
Mircea-Octavian Poenaru ◽  
Adrian Neacsu ◽  
Romina Marina Sima ◽  
...  

Anorectal atresia (ARA) is a common congenital anomaly, but prenatal diagnosis is difficult, late, and unspecific. Utilizing a case of a 46 year old primipara with an egg donation In Vitro Fertilization (IVF) pregnancy, diagnosed at the first trimester scan with an anechoic isolated structure, which indicates anal atresia, we performed a systematic literature review in order to evaluate early prenatal ARA diagnosis. A total of 16 cases were reported as first trimester ARA suspicion, and only three had no associated anomalies. The most frequent ultrasound (US) sign was the presence of a cystic, anechoic pelvic structure of mainly tubular shape, or a plain abdominal cyst. In the majority of cases, structures were thin-walled and delimitated from the bladder. The presence of hyperechoic spots signifying enterolithiasis and peristaltic movements were helpful in order to establish the bowel origin of the lesion. Considering the high eventuality that the lesion is transitory, meaning later in pregnancy the fetus looks normal, early detection of such a sign should prompt further structural detailed evaluation, karyotyping, and appropriate pregnancy and postnatal counselling.


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