Inflammatory myofibroblastic tumor (IMT) is an uncommon, usually benign, mesenchymal tumor. IMT affects people of all ages, but it more commonly occurs in children and adolescents. Also, has the potential to arise any part body, though, frequently develops lungs mesentery. In this report, we discuss a rare clinical manifestation mesenteric presented as intussusception small intestine 7-year-old child.

The presence of vermiform appendix in an inguinal hernia sac is known as Amyand's hernia. This research paper examines the case a 28-day-old Syrian male presented with history infected right-sided hydrocele from age 14 days. Upon admission, ultrasonography was reported right testicular torsion. Accordingly, emergency surgical exploration performed, and by exposing spermatic cord fascia, 7 mL pus drained, revealing cecum perforated lying beside testis, which showed evidence ischemia bluish...

Abstract Omphalopagus twins are one of many forms conjoined sharing part the gastrointestinal system and abdominal wall. This type has best chance survival if successfully separated. Surgical approaches in these cases generally preferably elective, but sometimes separation may be urgently needed due to life-threatening complications, such as hemodynamic instability, death either twin, necrotizing enterocolitis, among others. We report a case separated omphalopagus at day two life.

Lipomas are benign tumors composed of mature adipocytes. A 1-year-old-male baby was admitted to the hospital with a history an abdominal mass, which had been incidentally detected by local pediatrician. upon examining child for complaint distention and chronic diarrhea. An ultrasound computed tomography scan were performed, findings revealed fat confirmed laparotomy microscopic results. At laparotomy, soft yellow mass found attached mesentery jejunum. The enucleated without anastomosis,...

Urethral duplication is a rare congenital anomaly but more common in males, it can take many forms and presentations due to the anatomical positions histological epithelium of urethrae. In sagittal duplications, normal positioned dorsal urethra hypoplastic stenotic ventral one almost always one. We present case 4 years old boy highlights form dominant an accessory (type II A 2 Y according effmann classification) discuss its treatment.

Gastric duplication cysts (GDCs) are rare congenital anomalies. Presentation of GDCs varies from an asymptomatic abdominal mass to fulminant or massive gastrointestinal (GI) bleeding. Herein, we describe a case GDC in 10-month-old infant presenting with unexplained GI hemorrhage and hematemesis. An ultrasound was negative, while computerized tomography was, initially, inaccessible. Through series repeated esophagogastroduodenoscopies, documented penetration the into gastric cavity that later...

Intussusception (IS) is defined as invagination of part the bowel into an adjacent section intestines and second most common cause small obstruction in children. Postoperative ileoileal intussusception after surgical reduction a special type considered idiopathic. This research paper examines case female Syrian toddler who had been diagnosed with reduction. Diagnosis celiac disease was later histopathologically confirmed. Celiac (CD) may be underlying for types that idiopathic, further...

Acute appendicitis associated with ovarian epidermoid cyst torsion is extremely rare. To our knowledge, there are about 7 cases that have been reported in English literature, and was no any of them.Herein, we present the case a 2.5-year-old girl history vomiting, fever, abdominal pain. She prepared for operation following clinical radiological assessment. At laparotomy, left lesion were found. An appendectomy salpingo-oophorectomy performed complications occurring during surgery or follow-up...

Abstract Fetal intestinal volvulus is rare, but it a serious condition due to its life-threatening complications. The bowel loop becomes twisted; thus, impaired venous return leads necrosis. Prenatal most secondary atresia, arterial supply defect or without any underlying cause, with consideration that cystic fibrosis the cause of obstruction, because meconium ileus. We report case prenatal complicated perforation and peritonitis in context

Although symptomatic Mickel's Diverticulum (MD) in infants is rare, we report a case of perforated at birth full term male with signs peritoneal irritation. Because the rareness infants, predicting preoperative diagnosis so difficult, but it doesn't affect prognosis.

Intestinal diffuse ganglioneuromatosis is a rare, benign, neoplastic condition characterized by disseminated proliferation of neural elements. It has an established association with several systemic disorders including: multiple endocrine neoplasia IIB (MEN IIB) and von Recklinghausen’s disease. However, isolated GNs are very rare sporadic. We report case 6-year-old patient was referred to the emergency department due colon perforation during endoscopy. He then underwent sigmoidectomy...

The management of bladder exstrophy (BE) remains one the most significant challenges encountered by pediatric urologists despite improvements in operative techniques worldwide. Regardless surgical technique, timing primary closure a matter debate. initial may be performed within first 48-72 hours life or at ~6-12 weeks age. Delayed presentation until adolescence is extremely rare. However, due to lack awareness, and access healthcare along with poor socioeconomic conditions developing...

Pheochromocytoma is a rare catecholamine secreting tumor originating from the chromafine cells of adrenal medulla, so it an unusual cause surgical hypertension and extremely in pediatric population. we present case 12-year-old girl who had intracranial hemorrhage as first demonstration due to blood undiagnosed pheochromocytoma.

Corrosive substance ingestion is a very serious home accident, mostly common in developing countries. It frequently causes esophageal burns the acute stage and stricture, stenosis, even cancer chronic stage. Severe cases of caustic esophagitis may require replacement. We describe case balloon endoscopy dilation two-year-old girl with severe stricture esophagus resulting from accidental corrosive (strong alkaline liquid) which helped patient preserve prevent clinical complication development...

Abdominal distention and constipation in children can be challenging as clinical problems.The number of possible diagnoses is very large may related to rare surgical causes.It rarely caused by an annular pancreas.Early recognition essential for preventing delays management potential complications.Here we report a case incomplete pancreas presenting abdominal 1.5-year-old Syrian boy.The diagnosis was made through computed tomography scan (CT).

Congenital esophageal stenosis (ces) and Tracheo-esophageal fistula are rare types of congenital anomalies who have its origin in the embryological development trachea esophagus at sixth seventh weeks gestation. These often not diagnosed until months or sometimes years after birth. In this article we present you an unusual type proximal CES combined with TEF same level that was 5th day life.

Sternal cleft is a rare congenital malformation resulting from fusion failure of the sternum and often patients have no clinical signs at birth. The defect usually divided into partial or complete forms accompanied by other anomalies. We herein report case upper sternal that was repaired in neonatal period primary closure after thymectomy. patient discharged 9 days operation with good condition normal respiratory movements. case, little more than 100 cases published worldwide.