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APSP Journal of Case Reports

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https://www.readbyqxmd.com/read/28164005/urachal-cyst-meckel-s-diverticulum-and-band-and-urachus
#1
Dileep Garg, Aditya Pratap Singh, Sunil Kothari, Ayush Kumar
No abstract text is available yet for this article.
January 2017: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/28164004/atypical-presentation-of-multiple-foreign-body-ingestion
#2
Emrah Aydın, Sultan Bent, Burak Ayan
Foreign body ingestion is very common in childhood especially under 3 year of age. Pica syndrome is characterized by an appetite for substances that are largely non-nutritive. We present a 3-year old girl who presented to ER with symptoms and signs of intestinal obstruction.
January 2017: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/28164003/ingested-metallic-spool-a-rare-cause-of-acquired-tracheoesophageal-fistula
#3
Imran Hashim, Nabila Talat
Foreign body (FB) ingestion is a common problem in children. Prolonged impaction of FB in esophagus may result in tracheoesophageal fistula (TEF). A 6-year-old girl presented with progressive dysphagia and recurrent chest infections. No history of FB ingestion was given by parents. Further investigations revealed FB (spool) in cervical esophagus. Patient was successfully managed by surgery through trans-cervical approach.
January 2017: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/28164002/giant-omphalocele-complicated-by-postoperative-duodenal-obstruction
#4
Sunita Ojha, Shobha Parashar, Dharmil Doshi, Rajiv Kumar Bansal
Omphalocele is a congenital defect in the abdominal wall, usually treated at birth or within 1-2 years of life depending on condition of patient and size and contents of the defect. We repaired a giant omphalocele without mesh in a 9-year-old girl. She developed duodenal obstruction in the postoperative period requiring another laparotomy and duodeno-jejunostomy to bypass obstruction.
January 2017: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/28164001/abdominal-mass-secondary-to-human-toxocariasis
#5
Javad Ghoroobi, Leily Mohajerzadeh, Maliheh Khoddami, Alireza Mirshemirani, Naser Sadeghian, Alireza Mahdavi, Sayeh Hatefi
Toxocariasis is an extensive helminthic infection that leads to visceral larva migrans in humans. A 2.5-year-old girl referred for abdominal mass. She had history of pharyngitis for two weeks. There were no other symptoms. Abdominal examination revealed an irregular solid mass in right lower quadrant (RLQ). Abdominal ultrasonography revealed an echohetrogenic large mass in RLQ, liver, and retroperitoneal area. Abdominal CT scan showed a huge mass. At laparotomy a large retroperitoneal mass that involved right liver lobe, bladder, ileocecal valve, small and large intestines was found...
January 2017: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/28164000/spinal-dural-arteriovenous-fistula-and-cecal-arteriovenous-malformation-in-a-boy
#6
Vimlesh Soni, Pankaj C Vaidya, Jitendra Kumar Sahu, Mukesh Yadav, Pratibha Singhi
Concurrent spinal dural arteriovenous fistula (AVF) and cecal arteriovenous malformation (AVM) are very rare. A 6-year old boy presented with lower limb paresis after trauma. On imaging work-up spinal dural AVF was found. It was managed with endovascular glue embolization. After two years, the boy presented with severe anemia and occult gastrointestinal tract (GIT) bleed. Cecal AVM was diagnosed and managed with embolization.
January 2017: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/28163999/food-allergy-a-rare-cause-of-recurrent-intussusception
#7
Emrah Aydın, Ömer Faruk Beşer
Recurrent intussusception is a management dilemma and have many causes. We report a 22-month old boy who presented multiple times for recurrent intussusception. At diagnostic work-up he was found to be suffering from non-IgE food allergy. The child did not develop further episodes of intussusception after removal of allergenic diet.
January 2017: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/28163998/bilateral-cystic-adrenal-neuroblastoma-with-cystic-liver-metastasis
#8
Mine Aslan, Deniz Alis, Ayse Ucar Kalyoncu, Hatice Arioz Habibi, Gul Nihal Ozdemir, Basak Koc, Ibrahim Adaletli
Bilateral congenital cystic adrenal neuroblastoma (NB) with cystic liver metastasis is a very rare condition and only few cases have been reported in the literature. Herein we report a case of a congenital bilateral cystic adrenal NB with cystic liver metastasis and briefly discuss characteristic imaging features of cystic NB.
January 2017: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/27900283/giant-primary-epithelial-splenic-cyst-in-an-adolescent-girl
#9
Pradeep Kajal, Kamal Nain Rattan, Namita Bhutani, Kapil Bhalla
No abstract text is available yet for this article.
November 2016: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/27900282/severe-hematuria-and-prevesical-hematoma-after-open-ureterocystoneostomy-sequel-of-undiagnosed-hemophilia
#10
Eiji Hisamatsu, Kaoru Yoshino
No abstract text is available yet for this article.
November 2016: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/27900281/postoperative-ileocolic-intussusception-in-a-neonate-with-anorectal-malformation
#11
Piyush Kumar, Sudhir Singh, J D Rawat, Sarita Singh
No abstract text is available yet for this article.
November 2016: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/27900280/giant-lingual-teratoma-with-cleft-palate-in-male-new-born
#12
J D Rawat, Piyush Kumar, Sudhir Singh, Hemlata
No abstract text is available yet for this article.
November 2016: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/27900279/huge-gastric-teratoma-in-an-8-year-old-boy
#13
Rajpal S Sisodiya, Simmi K Ratan, Parveen K Man
Gastric teratoma is very rare tumor and usually presents in early infancy. An 8-year-old boy presented with a huge mass in abdomen extending from epigastrium to the pelvis. Ultrasound and CT scan of abdomen revealed a huge mass with solid and cystic components and internal calcifications. The preoperative diagnosis was a teratoma but not specifically gastric one. At operation, it was found to be gastric teratoma. The mass was excised completely with part of the stomach wall. The histopathology confirmed it to be mature gastric teratoma...
November 2016: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/27900278/metanephric-adenofibroma-masquerading-as-wilms-tumor
#14
Prince Raj, Ashwini Khanolkar, Yogesh Kumar Sarin
Metanephric adenofibroma is a rare, biphasic, benign tumor containing both stromal and epithelial components and could be potentially mistaken as Wilms' tumor (WT). We present a 5-year-old girl who was suspected to have metastatic Wilms' tumor on radiological investigations/tru-cut biopsy and had received neoadjuvant chemotherapy, but postoperatively final histopathology revealed it as metanephric adenofibroma. No postoperative chemotherapy was given.
November 2016: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/27900277/incidentally-diagnosed-multiple-vascular-lesions-of-the-spleen-littoral-cell-angioma-or-hemangioma
#15
Emrah Aydin
Vascular lesions of the solid abdominal viscera may pose diagnostic and management issues. A 16-year old girl admitted to emergency department due to recurrent abdominal pain and diagnosed to have multiple vascular malformations of the spleen on imaging investigations. Littoral cell angioma was preoperative suspicion owing to no response of the vascular lesion to the propranolol. It turned out to be cavernous hemangioma on histopathology.
November 2016: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/27900276/foreign-body-in-duodenum-mimicking-a-duplication-cyst-on-imaging
#16
Aditya Pratap Singh, Vinay Mathur, Ramesh Tanger, Arun Gupta, Ayush Kumar
Paediatric age group is most vulnerable for the accidental foreign body (FB) ingestion which may go unnoticed. These patients present with symptoms or complications as a result of FB and may mimic other conditions on various investigations. We describe a 9-month old infant who ingested crystal gel ball and presented with vomiting for a month. On radiological imaging it was interpreted as duplication cyst of the duodenum. At operation, crystal gel ball was retrieved. Our case vindicates importance of keeping various possibilities in mind as differential diagnoses during evaluation and management of surgical ailments such as the duplication cyst of duodenum...
November 2016: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/27672584/tetra-amelia-syndrome
#17
Shilpi Gupta, Vineeta Chaturvedi, Liladhar Agarwal
No abstract text is available yet for this article.
September 2016: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/27672583/malrotation-and-midgut-volvulus-associated-with-asymptomatic-duplication-cyst-of-jejunum
#18
Sandip Kumar Rahul, Vijai Datta Upadhyaya, Basant Kumar
Gastrointestinal duplications can affect any part of the alimentary tract and are notorious for their variable presentation. Their association with malrotation and midgut volvulus is rare. We describe an 8-year old boy presented with episodes of abdominal pain. Radiological workup showed whirlpool sign and abnormal relationship of mesenteric vessels. At operation, malrotation with chronic volvulus was found. Incidentally, a jejunal communicating duplication cyst was also noted.
September 2016: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/27672582/neurenteric-cyst-presenting-with-bleeding-per-rectum
#19
Taruna Yadav, Padam Parmar, Kamal Nain Rattan
Neurenteric cyst in the thoracic cavity may produce a myriad of clinical features. We report a 7-month-old girl who presented with significant bleeding per rectum. On imaging, a mediastinal cystic structure with air-fluid levels was evident with cervico-thoracic vertebral anomalies. The cyst was excised and histopathology showed intestinal mucosal lining with heterotopic pancreatic tissue confirming the diagnosis of neurenteric cyst.
September 2016: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/27672581/symptomatic-mullerian-duct-cyst-in-a-male-infant
#20
Abhishek Chinya, Prince Raj, Shandip Kumar Sinha, Yogesh Kumar Sarin
Symptomatic Mullerian duct cyst is a rare entity in children. A 9-month-old male infant presented with bowel and urinary obstructive symptoms. Imaging investigations revealed a cystic mass in the rectovesical pouch compressing bladder neck and rectum. At laparotomy, a Mullerian duct cyst was found. Most of the cyst was excised and the remaining cyst mucosa was cauterized. The child improved thereafter.
September 2016: APSP Journal of Case Reports
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