Perforated Meckel's diverticulum in a 6-day-old neonate: A case report.

Introduction And Importance: Meckel's diverticulum is The most common congenital anomaly of the gastrointestinal tract, Meckel's diverticulum, affects around 2 % of the general population. Meckel's diverticulum symptoms in the newborn stage are quite uncommon.

Case Presentation: A male newborn, aged 6 days, was brought to our hospital due to recurrent episodes of vomiting during nursing and fever.

Intestinal obstruction due to giant liver cyst: A case report.

Background: Congenital hepatic cysts are relatively rare but are now diagnosed earlier and more frequently with a routine prenatal ultrasound. Solitary liver cysts are divided into simple and solitary intrahepatic biliary cysts, depending on the biliary connection. While some solitary liver cysts are symptomatic in childhood, even in newborns, they are often found incidentally in adults.

A strangulated umbilical hernia with perforated Meckel diverticulum: Case report.

Introduction And Importance: Meckel's diverticulum (MD) is one of the most common gastrointestinal anomalies and affects 2-3 % of the population. Strangulated umbilical hernia with a perforated Meckel diverticulum is an extremely rare event.

Case Presentation: We reported here a case of one year old boy of a strangulated umbilical hernia with perforated MD that operated at the Mogadishu hospital.

Spontaneous rupture of umbilical hernia with evisceration of small bowel in an infant: A case report.

Introduction: Umbilical hernia is a condition that frequently affects children, with the majority resolving spontaneously. The appearance of redness, ulceration, or a sudden increase in the size of the umbilical hernia is indicative of a threatening rupture and suggests the requirement for surgical intervention. We hereby present a case of spontaneous umbilical hernia rupture with bowel evisceration.

Infantile Bowel Obstruction in a Patient with Situs Inversus Totalis and Polysplenia: A Case Report.

The infantile intestinal obstruction associated with situs inversus totalis and polysplenia is extremely rare, with only a few cases reported in the literature. Furthermore, the management of this association is complicated. We report a case of a 2-month-old boy with intestinal obstruction due to malrotation and volvulus with thin translucent omentum sac encasing the small intestine associated with situs inversus totalis, polysplenia, and pulmonary hypertension.

Retrospective evaluation of inpatients admitted to a tertiary hospital in Somalia for Pediatric surgery.

Objective: The aim is to reflect on the epidemiology of the patient population at a tertiary hospital for pediatric surgery, diagnostic pattern, and mortality in Somalia retrospectively.

Methods: In this study, 163 patient who were hospitalized to Pediatric Surgery Clinic of Mogadishu Somalia Turkey Recep Tayyip Erdoğan Training and Research Hospital in 2018 were included. Data regarding age, gender, diagnosis, surgical condition, mortality rate and cause of the death were recorded from the patient charts and the institutional digital database.

A case of empyema necessitans in an adolescent with mycobacterium tuberculosis.

Introduction And Importance: An empyema is a buildup of pus in the pleural space and is most commonly associated with pneumonia. Streptococcus pneumonia is the most common cause of pneumonia, although staphylococcus aureus is common in developing countries. empyema necsitans is An extravasation of purulent material outside the pleural space involving the chest wall.

Rare case cystic scrotal lymphangioma presented as a hydrocele.

Introduction And Importance: Cystic scrotal lymphangiomas are very uncommon lesions caused by congenital lymphatic malformation. These tumors are usually located in the neck and axilla, occasionally in the mediastinum, retroperitoneum, and thigh. The scrotum and perineum are the least frequented sites.

Waardenburg-Shah syndrome rare and challenging case report from Somalia.

Introduction And Importance: Waardenburg-Shah disorder could be an uncommon autosomal recessive inherited ailment characterized by aganglionic megacolon with a high mortality rate. Babies born with Waardenburg syndrome may have typical features of hair, skin and eye pigmentary abnormalities, and hearing loss. Here we present a case with typical presentation of Waardenburg Shah syndrome.