1.Eltrombopag-Induced Near-Fatal Hyperammonemic Encephalopathy – Case Report
Patrick TOMLINSON ; Barbara PAQUETE ; Jessica GREEN ; Bianca Maria GOFFREDO ; Ehab HAMOUDA ; Katya BENNETT ; Bernd C. SCHWAHN
Clinical Pediatric Hematology-Oncology 2026;33(1):39-44
An 8-year-old girl with chronic immune thrombocytopenic purpura treated with eltrombopag presented with lactic acidosis and severe hyperammonemic encephalopathy necessitating hemofiltration. Genetic metabolic disorders associated with hyperammonemia were excluded. Despite standard dosing, supratherapeutic plasma levels of eltrombopag were found, suggesting an adverse drug effect due to drug accumulation. Awareness of hyperammonemia as adverse reaction to eltrombopag is warranted. Close monitoring of transaminases is required in children and therapeutic drug monitoring could aid in tailoring effective treatment doses for children to mitigate risk in populations that are more susceptible to complications.
2.A Case of a Child with Undescended Left Testis Presenting with Acute Right Scrotal Swelling.
Shi Yuan WANG ; Ehab Shaban Mahmoud HAMOUDA
Annals of the Academy of Medicine, Singapore 2018;47(2):85-87
Cryptorchidism
;
diagnosis
;
Hernia, Inguinal
;
diagnosis
;
Humans
;
Infant
;
Male
;
Scrotum
;
pathology
;
Ultrasonography
3.Simultaneous Omental Infarction and Acute Appendicitis in A Child
Koay Hean Tang ; Hamouda Ehab Shaban Mahmoud
The Medical Journal of Malaysia 2015;70(1):42-44
It is crucial to realize that both omental infarction and acute
appendicitis can occur simultaneously in the children as
both diseases are managed differently. Omental infarction
itself is rare in the pediatric group, and its association with
acute appendicitis is even rarer. Both diseases usually
present with right sided abdominal pain. Ultrasound is the
choice of imaging modality in the investigation of abdominal
pain in the children. It should not be content if omental
infarction is detected, whilst the normal appendix is not
seen. We reported a case of simultaneous omental infarction
and acute appendicitis in a child who presented with 3 days
history of right sided abdominal pain. It was diagnosed preoperatively
by ultrasound. Prompt surgical intervention was
proceeded and the child made uneventful recovery.
Appendicitis
;
Infarction
4.Enlarged parietal foramina presenting as scalp swelling in an infant
Chidambaram Viswanath Anand ; Hamouda Ehab Shaban Mahmoud
The Medical Journal of Malaysia 2015;70(4):263-264
“Enlarged parietal foramina” is a congenital malformation
with autosomal dominant inheritance. The condition is
usually self-limiting and doesn’t require any treatment.
However, it may also be associated with encephalocele,
vascular anomalies or may be a part of syndrome. We
present a case of enlarged parietal foramina in a child and
discuss its imaging findings and the associated intracranial
vascular malformations.
Encephalocele

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