INTRODUCTION Colonic atresia and anorectal malformation are rare congenital anomalies individually. Few reports of the conditions combined in a single patient have been published in the literature. Neither colonic atresia, anorectal malformation or a combination of the disorders has previously been reported in the Haitian population. CASE PRESENTATION A 5-day-old female presented with feculen...

The Chiari malformation is an infrequently detected congenital anomaly characterized by the downward displacement of the cerebellum with a tonsillar herniation below the foramen magnum that may be accompanied by either syringomyelia or hydrocephalus. Surgery, such as foramen magnum decompression, is indicated for a symptomatic Chiari malformation, although an incidental lesion may be followed-u...

An abnormal origin of the ophthalmic artery from the basilar artery, found in conjunction with an orbital arteriovenous malformation, is described. The successful treatment of the arteriovenous malformation by embolization through the ophthalmic artery is also reported.

A case of arteriovenous malformation of the left cerebellopontine angle causing symptoms of ipsilateral trigeminal neuralgia is reported. Pain relief followed microsurgical removal of the malformation. The authors review the literature on the subject.

A child with the antenatal diagnosis of pulmonary cystic adenomatoid malformation underwent thoracotomy and an intralobar bronchopulmonary sequestration was found. Histological examination of the resected specimen showed cystic adenomatoid malformation within the sequestered segment.

in this report we introduce two cases of penile agenesis. the first case was a newborn with male appearance and a well developed scrotum containing two normal testes, but the penis and urethral meatus were absent. the bladder was connected to the rectum by an intra-abdominal canal. the second case was a premature newbron of 32 weeks, who died in the first day of life. in addition to penile agen...

Background: Hirschsprung’s disease is a genetic disorder characterized by the absence of ganglion cells in different lengths intestine. It one common causes intestinal obstruction neonates.
 Materials and Methods: The study was carried out from January 2017 to 2020 Department Pathology Tertiary care hospital. biopsy specimens spastic segment colostomy or ileostomy sites were sent for evalu...

Pulmonary arteriovenous (A-V) malformation is frequently a manifestation of Osler-Weber-Rendu syndrome (hereditary hemorrhagic telangiectasia). We identified 14 patients (9 men and 5 women) with A-V malformation by contrast echocardiography; 10 patients with atrial right-to-left shunt served as control subjects. Agitated saline solution (10 ml) was injected through a peripheral vein during echo...

BACKGROUND Patients with pulmonary arteriovenous malformations usually complain of dyspnoea upon exertion, fatigue or migraine, or may be asymptomatic. We describe a patient with an unreported manifestation of a pulmonary arteriovenous malformation: a severe chronic cough. CASE PRESENTATION A 51-year old Caucasian non-smoking female police officer presented with a chronic cough. She had been ...

Background: Spinal dural AVF is the most common type of spinal vascular malformation. However, presenting symptoms differ according to site of spinal involvement. This study described a case of arteriovenous malformation with paraparesis and incontinence. Case Presentation: Diagnosis of patient was confirmed by clinical and imaging examination using magnetic resonance image and ruling out ot...