Temporary Neurological Symptoms, Headache and Csf Iymphocytosis-HaNDL Syndrome

EBRU APAYDIN DOGAN, FİGEN GÜNEY, EMİNE GENÇ, MUZAFFER MUTLUER, Nurhan İlhan

  • EBRU APAYDIN DOGAN: SELCUK ÜNV MERAM TIP FAK
  • FİGEN GÜNEY: NECMETTİN ERBAKAN ÜNİVERSİTESİ
  • EMİNE GENÇ: NECMETTİN ERBAKAN ÜNİVERSİTESİ TIP FAKÜLTESİ
  • MUZAFFER MUTLUER: KARAMAN DEVLET HASTANESİ
  • Nurhan İlhan: Selçuk Üniversitesi Meram Tıp Fakültesi
  • Year : 2008
  • Vol : 24
  • Issue : 4
  •  Page : 227-229
Aim: In this case report, it is aimed to discuss the ‘HaNDL Syndrome’ with the relevant literature. Case Report: A 20 year-old woman was admitted to the emergency department with left-sided, severe, throbbing headache accompanied with nausea, vomitting, sonophophia and phonophophia. Approximately 30 minutes after the pain emerged, she had suffered numbness and mild paresis on the right side of the body including the right side of her face accompanied with difficulty in speech which improved in approximately 20-25 minutes. She reported that 2 weeks prior these symptoms, she had suffered severe nausea and diarrhea that had lasted for 3 days. A diagnosis of viral gastroenteritis had been made and supportive therapy had been advised by a doctor. In the clinic, spinal tap was performed which revealed lymphocytic pleocytosis and mild elevation of protein level (49 mg/dL). Brain computerized tomography and the contast MR were normal. After the exclusion of other conditions which may cause CSF pleocytosis and severe headache; a diagnosis of HaNDL Syndrome was made. Conclusion: Recognition of this bening syndrome, is important as performing a diagnostic angiography may cause severe complications.

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Conflict of interest : Yok
Selcuk Medical Journal
2008, Vol. 24 (4)
ISSN: 1017-6616
E-ISSN: 2149-8059
Received : , Accepted : , Published Online :