Pediatric acute-onset neuropsychiatric syndrome in a 6.5-year-old boy: A case report

Authors

  • Arman Masoudi Department of psychiatric diseases, Yahyanejad hospital, school of medicine, Babol university of medical sciences, Babol, Iran
  • Ehsan Abiri Non-communicable pediatric diseases research center, Babol university of medical sciences, Babol, IR Iran
  • Mahmoud Khodabandeh Division of infectious diseases, children’s medical center, pediatrics’ center of excellence, Tehran university of medical sciences, Tehran, Iran
  • Mohsen Mohammadi Non-communicable pediatric diseases research center, Babol university of medical sciences, Babol, IR Iran
Abstract:

Background: “Pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections”, or PANDAS, is a syndrome characterized by acute-onset obsessive-compulsive disorder (OCD) and/or tics accompanied by the neuropsychiatric symptoms. This case is reported because of its rarity. Case report: A 6.5-year-old boy with swollen tonsils, high-grade fever and rash was admitted to Amirkola Children’s Hospital, Northern Iran. Thereafter he got involved with tachycardia, hypotension, suppurative conjunctivitis and swelling of extensor surfaces of extremities. In addition, after the onset of fever, he had some neuropsychiatric problems such as social isolation, irritability, aggression, oppositional behavior, behavioral regress, unusual sound production, repeated vilifications, loss of appetite and handwriting deterioration. He was treated with intravenous immunoglobulin (IVIG). The patient was discharged from the hospital in a good condition. Conclusions: The medical treatment of underlying disease leads to remarkable patient's neuropsychological and OCD symptoms. PANDAS should be diagnosed in the streptococcal infections associated with abrupt behavioral symptoms and treated with IVIG and antibiotics.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

Xanthogranulomatous pyelonephritis report of a case in a 5 year old boy

Xanthogranulomatous pyelonephritis is an unusual type of the kidney infection which is characterized by infiltration of mononuclear inflammatory cells and lipid laden macrophages ( foam cells). It is manifested by a firm, lobulated and yellowish kidney mass which is difficult to differentiate from renal cell carcinoma grossly. Six out of 1000 cases of cryonic pyelonephritis which are treated su...

full text

sudden onset monoparesis and dysarthria in a 5-year-old boy: a case report

case presentation we report a 5-year-old boy, who was presented with sudden right hand monoparesis and dysarthria. conclusions the patient was investigated with magnetic resonance angiography and diagnosed as md. introduction moyamoya disease (md) is a disorder caused by blocked arteries at the base of the brain. as the normal blood vessels narrow and become blocked, a person may suffer a strok...

full text

A 30-year-old healthy man with recent onset erythromelalgia: A case report

A 30-year-old healthy man came to our hospital with complaints of red, hot, and painful upper extremities which spontaneously appeared. These manifestations worsened with exercises and heat, but were alleviated by rest and cooling of the hands. There were 2 similar previous episodes of short duration. The patient was a healthy, non-alcoholic, non-smoker with no history of using medicine. ...

full text

Acute Flaccid Myelitis in A 9- year- old Girl: A Case Report

Acute Flaccid Myelitis (AFM), a polio-like paralysis in children no older than 21, has recently reemerged and increasing numbers of such cases have been reported worldwide since 2012. Accurate and early diagnosis of this condition could help with better management of the disease. A 9- year- old girl with chief complaint of headache, fever and vomiting was subsequently affected by an acute...

full text

Autoimmune Polyglandular Syndrome Type 2 (APS-2) in a 70-Year-Old Woman: A Case Report

Type2 autoimmune polyglandular (Schmidt) syndrome is defined by the occurrence of at least 2 out of 3 of the following manifestations, Addison's disease, Hypothyroidism and Type 1 diabetes mellitus. APS2 is a rare condition with an incidence of 1–2/100 000 per year. Prevalence of APS-2 is most happening in the range of 20-40 years of age. Here we present a patient who complained about loss of ...

full text

Case Report Complete Diphallus in a 14-year-old Boy

We herein present an unusual case of 14-year-old boy with complete diphallus and bifid scrotum. He was not aware of his extragenital abnormality until he was examined by a surgeon before circumsion. During surgery, the hypoplastic penis was resected and a single scrotum was constructed by removing the band of skin separating the compartments. The rugose skin was then joined, giving scrotal cont...

full text

My Resources

Save resource for easier access later

Save to my library Already added to my library

{@ msg_add @}


Journal title

volume 5  issue 1

pages  325- 328

publication date 2019-03

By following a journal you will be notified via email when a new issue of this journal is published.

Keywords

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023