1.A case of continuous-type splenogonadal fusion.
Jasin Arachchige Saman Bingumal JAYASUNDARA ; Vithanage Hasanthi VITHANA ; Ananda Kumara LAMAHEWAGE
Singapore medical journal 2013;54(6):e123-4
Splenogonadal fusion is a rare developmental anomaly in which an abnormal connection between the splenic tissue and gonads or mesonephric derivatives is present. Less than 200 cases have been reported since it was first described in 1883. Preoperative misdiagnosis is common and may lead to unnecessary orchidectomy if testicular neoplasm is suspected. To avoid such outcomes, it is important to be aware of the features of splenogonadal fusion. We report the case of a five-month-old male infant with continuous-type, left-sided splenogonadal fusion, which was discovered during groin exploration for a scrotal mass. Although the lesion was first noted during an episode of nonspecific viral fever, such an association is uncommon. Preoperative ultrasonographic evaluation favoured a diagnosis of a large haemangioma. This is the first reported case of splenogonadal fusion from Sri Lanka.
Diagnosis, Differential
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Humans
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Infant
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Male
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Spleen
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abnormalities
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surgery
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Splenic Diseases
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diagnosis
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surgery
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Testicular Diseases
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diagnosis
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surgery
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Testis
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abnormalities
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surgery
2.Organoaxial partial rotation of duodenum with midgut malrotation in an adult.
Luckshika Udeshani AMARAKOON ; Baj Gamage Anushka RATHNAMALI ; Jasin Arachchige Saman Bingumal JAYASUNDARA ; Ajith de SILVA
Singapore medical journal 2014;55(12):e191-3
Midgut malrotation includes a range of developmental abnormalities that occur during fetal intestinal rotation. Manifestations of intestinal malrotation are generally seen in the paediatric population and are uncommon in adults. Symptomatic patients may present with either acute abdominal pain due to midgut volvulus, or chronic abdominal pain due to proximal midgut partial obstruction in the presence of congenital bands. A limited number of paediatric cases of duodenal occlusion due to duodenal malrotation has been previously reported in the medical literature. We herein report the case of a 57-year-old woman who presented with duodenal obstruction due to organoaxial partial rotation of the distal duodenum associated with midgut malrotation. This is probably the first of such a case diagnosed in adulthood reported in the medical literature. Our patient underwent Roux-en-Y duodenojejunostomy and had symptomatic relief following the successful surgery.
Duodenal Obstruction
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congenital
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diagnosis
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surgery
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Duodenostomy
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Duodenum
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abnormalities
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Female
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Humans
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Middle Aged
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Sri Lanka
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Treatment Outcome