A RARE CASE OF ACUTE MOTOR AXONAL NEUROPATHY IN A ONE-YEAR-OLD MALE CHILD Acute Motor Axonal Neuropathy (AMAN), a major subtype of Guillain Barre’s Syndrome (GBS), is a rare non-inflammatory disease where the axons of motor neurons are selectively targeted by the immune system. This report describes the case of a one-year-old male suffering from this rare condition. The patient presented with complaints of bilateral lower and upper limb weakness, accompanied by fever. Clinical and electromyographic investigations confirmed the diagnosis as AMAN. Treatment included intravenous immunoglobulin (IVIg), antibiotics, multivitamins, zinc, and physiotherapy, which led to significant improvement in the patient’s condition. Early diagnosis, along with prompt initiation of IVIg and physiotherapy, may greatly enhance recovery from GBS-AMAN in pediatric patients.

BACKGROUND/AIMS: To investigate the various etiologies, yields, and effects of capsule endoscopy (CE) on management and complications, along with follow up of patients with obscure gastrointestinal (GI) bleeding. METHODS: The study group of patients included those having obscure, overt, or occult GI bleeding. The findings were categorized as (A) obvious/definitive, (B) equivocal, or (C) negative. Any significant alteration in patient management post CE in the form of drug or surgical intervention was noted. RESULTS: Total patients included in the study were 68 (48 males and 20 females). The ratio of male:female was 2.4:1. The age ranged between 16 years to 77 years. Mean age for males was 62+/-14 years, for females 58+/-16 years. The total yield of CE with definitive lesions was in 44/68 (65.0%) of patients. In descending order (A) angiodysplasia 16/68 (23.53%), (B) Crohn's disease 10/68 (14.70%), (C) non-steroidal anti-inflammatory drug enteropathy 8/68 (11.76%), (D) small bowel ulcers 4/68 (5.88%), (E) jejunal and ileal polyps 2/68 (2.94%), (F) intestinal lymphangiectasis 2/68 (2.94%), and (G) ileal hemangiomas 2/68 (2.94%) were followed. Equivocal findings 12/68 (17.65%) and negative study 12/68 (17.65%) was found. Complications in the form of capsule retention in the distal ileum were noted in 2/68 (2.94%) subjects. Statistically, there was a higher probability of finding the etiology if the CE was done during an episode of bleeding. CONCLUSIONS: CE plays an important role in diagnosing etiologies of obscure GI bleeding. Its role in influencing the management outcome is vital.
Angiodysplasia ; Capsule Endoscopy* ; Crohn Disease ; Diagnosis* ; Female ; Follow-Up Studies ; Hemangioma ; Hemorrhage* ; Humans ; Ileum ; Lymphangiectasis, Intestinal ; Male ; Polyps ; Ulcer

Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is an extremely rare, potentially fatal, congenital anomaly with a high mortality rate in the first year of life. It occurs rarely in adulthood and may appear with malignant ventricular a rrhythmia or sudden death. We report a case of a 49-year-old woman with ALCAPA who presented with dyspnea on exertion. Management was coronary artery bypass grafting to the left anterior descending artery and obtuse marginal arteries, closure of the left main coronary artery ostium, and reestablishment of the dual coronary artery system.
Arteries ; Bland White Garland Syndrome ; Cardiopulmonary Bypass ; Coronary Artery Bypass ; Coronary Vessels* ; Death, Sudden ; Dyspnea ; Female ; Humans ; Middle Aged ; Mortality ; Pulmonary Artery*