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APSP Journal of Case Reports

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https://www.readbyqxmd.com/read/27900283/giant-primary-epithelial-splenic-cyst-in-an-adolescent-girl
#1
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
#2
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
#3
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
#4
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
#5
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
#6
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
#7
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
#8
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
#9
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
#10
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
#11
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
#12
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
https://www.readbyqxmd.com/read/27672580/right-parotid-fibrolipoma-a-rare-lesion-in-a-child
#13
Kamal Nain Rattan, Sunita Singh, Shruti Bansal
Lipoma rarely involves parotid gland especially in children. An 11-year-old boy presented with right parotid swelling. Preoperative workup including CT scan and FNAC gave suspicion of parotid gland lipoma. The diagnosis was confirmed on histopathology after complete excision of the mass.
September 2016: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/27672579/disc-battery-an-unusual-vaginal-foreign-body-in-a-child
#14
Yousuf Aziz Khan, Mansoor Mahmood, Esmaeel Taqi
Disc battery ingestion and esophageal injury is well-known in children. Insertion of a disc/lithium battery into body's natural orifices is rarely reported. We present a case of self-insertion of a lithium battery into the vagina by a 2 ½ year old female. Vaginoscopy was performed and the battery was retrieved which had corroded and caused vaginal ulceration. Post-operative outcome was favorable. Treating physicians must be aware of the hazardous effects of insertion of lithium batteries as it may cause significant damage in a short period...
September 2016: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/27672578/inflammatory-myofibroblastic-tumor-of-common-bile-duct-in-a-girl
#15
Aureen D'Cunha, Susan Jehangir, Reju Thomas
Inflammatory myofibroblastic tumor (IMT) is a rare, low grade malignant lesion which can occur anywhere in the body. In children it is usually found in the visceral soft tissues with a potential for local invasion and recurrence, and rarely distant metastasis. We report the diagnostic dilemma faced in the management of a 12-year old girl who presented with obstructive jaundice with a mass lesion at the distal end of the common bile duct. She underwent a tumor resection with a bilio-enteric bypass followed by a course of oral steroids and celecoxib...
September 2016: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/27672577/retained-wireless-capsule-endoscope-in-a-girl-with-suspected-crohn-s-disease
#16
Koushik Herle, Susan Jehangir
Wireless capsule endoscopy (WCE) is one of the great milestones in the field of gastroenterology. It is versatile in image acquisition, painless and can reach parts of the small bowel not amenable to conventional endoscopy. The commonest complication with WCE is retention of the capsule. We report a case of retained capsule in a child who was being investigated for obscure gastrointestinal bleeding (OGIB). Operative intervention was required for its retrieval after two weeks of expectant management.
September 2016: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/27398327/sacrococcygeal-teratoma-mistreated-with-repeated-aspirations
#17
Ramagopal G, Guru R, Suresh P, Moorthy G, Devi Lu
No abstract text is available yet for this article.
July 2016: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/27398326/intestinal-perforation-in-obstructed-umbilical-hernia-due-to-wedged-plum-seed
#18
Rahul Gupta, Vikram Singh Mujalde, Shilpi Gupta, Pradeep Kumar Gupta, Anu Bhandari, Praveen Mathur
The foreign body ingestion is a rare cause of gastrointestinal perforation in children and is typically seen with sharp foreign bodies or button batteries. Herein, we report an 11-month old male baby who presented with obstructed umbilical hernia. Abdominal radiograph showed dilated small bowel loops, while ultrasonography and CT scan suggested presence of a foreign body. Laparotomy revealed obstructed umbilical hernia with a plum seed being stuck in the terminal ileum causing intestinal perforation. Resection and anastomosis of intestine was performed...
July 2016: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/27398325/preduodenal-portal-vein-with-situs-inversus-totalis-causing-duodenal-obstruction
#19
Flavia D'souza, Amol Nage, Pradnya Bendre
Congenital duodenal obstruction sometimes may be secondary to unusual entities like preduodenal portal vein (PDPV) the identification of which is very important to avoid inadvertent injury or incorrect surgery. A 6-day old neonate presented with congenital duodenal obstruction. Investigations revealed situs inversus totalis with many congenital cardiovascular anomalies. At operation preduodenal portal vein and malrotation were found. Correction of malrotation and bypass duodeno-duodenostomy were done.
July 2016: APSP Journal of Case Reports
https://www.readbyqxmd.com/read/27398324/infantile-fibrosarcoma-of-tongue-a-rare-tumor
#20
Fazal I Wahid, Bakht Zada, Gul Rafique
Infantile fibrosarcoma is very rare tumor and seldom occurs in oral cavity. Overall good prognosis is reported in more than 80% cases. We present a 5-month old female patient with swelling of the tongue for four months. This was excised completely. Histopathology and immunohistochemistry revealed it as infantile fibrosarcoma of grade II.
July 2016: APSP Journal of Case Reports
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