Alice in Wonderland Syndrome: An Uncommon Presentation of Pyogenic Cerebral Abscess

Authors

  • Ayesha Abdul Samad Liaquat National Hospital and Medical College
  • Saba Zaidi Liaquat National Hospital, Karachi
  • Muhammad Luqman Liaquat National Hospital, Karachi

DOI:

https://doi.org/10.36283/ziun-pjmd13-4/025

Keywords:

Alice in wonderland, middle-aged, Perceptual disorder, Occipital lobe, Brain abscess

Abstract

Alice in Wonderland syndrome (AIWS) is a rare perceptual disorder causing distorted body image and spatial awareness. This is the case of a middle-aged man, known case of diabetes, hypertension, and chronic kidney disease who presented with a week-long history of fever, drowsiness, and visual hallucinations of unfamiliar people appearing unusually tall or short. He exhibited unusual behavior, frequently touching his nose and eyes as if they were unfamiliar or altered in some way. MRI revealed a ring-enhancing lesion in the left parieto-occipital region, indicating a brain abscess. He was treated with broad-spectrum antibiotics, steroids, and antifungal therapy due to his compromised immune state. On improvement of neurological symptoms, we discharged him with follow up in clinic. Our case addresses an uncommon exhibition of pyogenic cerebral abscess as AIWS. This highlights the importance of understanding of pathophysiology and contributes to the better understanding of such symptoms for similar cases in future.

Author Biographies

  • Ayesha Abdul Samad, Liaquat National Hospital and Medical College

    Neurology Department

  • Saba Zaidi, Liaquat National Hospital, Karachi

    Neurology Department

  • Muhammad Luqman, Liaquat National Hospital, Karachi

    Neurology Department

References

G Lerner A, Lev-Ran S. LSD-associated "Alice in Wonderland Syndrome"(AIWS): A Hallucinogen Persisting Perception Disorder (HPPD) Case Report. Isr J Psychiatry Relat Sci. 2015;52(1):67-8.

Farooq O, Fine EJ. Alice in Wonderland Syndrome: A Historical and Medical Review. Pediatr Neurol. 2017 Dec;77:5-11. doi: 10.1016/j.pediatrneurol.2017.08.008.

Fine E, Farooq O, Finnegan S, Zambrano M, Nasser M. Alice in Wonderland Syndrome: Case series and analysis (P4. 6-030).

Blom JD. Alice in Wonderland syndrome: A systematic review. Neurol Clin Pract. 2016 Jun;6(3):259-270. doi: 10.1212/CPJ.0000000000000251.

Lipsanen T, Lauerma H, Peltola P, Kallio S. Visual distortions and dissociation. J Nerv Ment Dis 1999;187:109–112.

Deecke L, Mergner T, Plester D. Tullio phenomenon with torsion of the eyes and subjective tilt of the visual surround. Ann N Y Acad Sci. 1981;374:650-5. doi: 10.1111/j.1749-6632.1981.tb30908.x.

Ffytche DH, Blom JD, Catani M. Disorders of visual perception. J Neurol Neurosurg Psychiatry. 2010;81:1280-7

Gencoglu EA, Alehan F, Erol I, Koyuncu A, Aras M. Brain SPECT findings in a patient with Alice in Wonderland syndrome. Clin Nucl Med. 2005;30:758-9.

Blom JD, Sommer IE, Koops S, Sacks OW. Prosopometamorphopsia and facial hallucinations. Lancet. 2014 Nov 29;384(9958):1998. doi: 10.1016/S0140-6736(14)61690-1.

Mastria G, Mancini V, Viganò A, Di Piero V. Alice in Wonderland Syndrome: A Clinical and Pathophysiological Review. Biomed Res Int. 2016;2016:8243145. doi: 10.1155/2016/8243145.

Liu AM, Liu JG, Liu GW, Liu GT. "Alice in Wonderland" syndrome: presenting and follow-up characteristics. Pediatr Neurol. 2014 Sep;51(3):317-20. doi: 10.1016/j.pediatrneurol.2014.04.007.

Oct-Dec 2024

Downloads

Published

2024-10-24

How to Cite

1.
Samad AA, Zaidi S, Luqman M. Alice in Wonderland Syndrome: An Uncommon Presentation of Pyogenic Cerebral Abscess. PJMD [Internet]. 2024 Oct. 24 [cited 2025 Jan. 25];13(4):198-202. Available from: https://ojs.zu.edu.pk/pjmd/article/view/2585

Similar Articles

1-10 of 124

You may also start an advanced similarity search for this article.