Cerebral Hydatid Disease Patients Admitted to Duhok City Hospitals: Management and Outcome

Authors

  • Walid Wahaib Al-Rawi M.B.Ch.B. (Baghdad), F.R.C.S. (Glasgow), Professor of Neurosurgery, College of Medicine, University of Duhok, Senior Consultant Neurosurgeon, Accident and Emergency Hospital (Teaching), Duhok City, Region of Kurdistan, Iraq.
  • Fatima Walid Al-Rawi M.B.Ch.B. F.R.C.S.O. (Glasgow), M.R.C.S.O. (Ireland), C.A.B.O., I.C.O. (London), Specialist Ophthalmologist, Eye Hospital (Teaching), Duhok City, Region of Kurdistan, Iraq

DOI:

https://doi.org/10.56056/amj.2023.214

Keywords:

Albendazole, Hydatid cyst absces, Recurrent cerebral hydatid cyst, Single cerebral hydatid cyst

Abstract

Background and objectives: The human systemic infestation with Echinococcus granulosus affects the brain in 2% of cases, cerebral hydatid cyst, which presents clinically as slowly growing intracranial mass lesion leading to variable symptomatology of raised intracranial pressure, neurological deficit, and epilepsy. The condition, when occurs, needs prompt surgical removal in order to avoid fatal consequences. The aim of this article is to report clinical data and our experience concerning cerebral hydatid cyst presentation, surgical management, complications, and outcome.

Methods: A retrospective case-series study encompassing 8 patients, four females and four males, whose ages ranged between 3.5-35 years, harboring cerebral hydatid cysts, including one cerebral hydatid abscess. The current study was conducted at Duhok Teaching Hospitals, during January 2005-May 2021. The diagnosis was established on clinical and radiological, computed tomography and magnetic resonance imaging backgrounds, and confirmed by operative findings, and histopathology (abscess cyst). Via appropriate craniotomies, all cerebral hydatid cysts, and abscess, were successfully removed, except, the recurrent hydatid cysts which needed an additional posterior fossa craniectomy to achieve total removal. There was no need for the use of advanced statistical system.

Results: Compared to their original neurological deficit at presentation, seven cases could achieve complete recovery, except, the patient with recurrence, whose recovery was delayed and suboptimal due to repeated surgeries; there was no mortality.

Conclusion: The operating surgeon should practice meticulous care avoiding the possible risk of an accidental rupture during cyst delivery. Various opinions address the pre-operative, intra-operative and post-operative use of Albendazloe, however, we are not sure whether the use of this medication could have prevented the recurrence of CHC which followed the accidental rupture.

Downloads

Download data is not yet available.

References

Alghoury A, El-Hamshary E, Azazy A, Hussein E, Rayan H Z. Hydatid Disease in Yemeni Patients attending Public and Private Hospitals in Sana’a City, Yemen. Oman Med. J. 2010; 25: 88-90.

Iraqi W. Diagnostic value of semi-purified antigens of hydatid cyst fluid in human cystic echinococcosis. Acta Parasitol. 2016; 61:144-50.

Yildiz K, Gurcan IS. The Detection of Echinococcus granulosus Strains Using Larval Rostellar Hook Morphometry. Turk. Parazitol Dergisi. 2009; 33: 199 – 2.

EL-Shazly A, Ranya MS, Usama SB, Tarek S, Hytham AZ. Evaluation of ELISA and IHAT in serological diagnosis of proven of human Hydatidosis. J. Egypt Soc. Parasitol. 2010; 40: 531 – 8.

Al-Abbassy SN, Altaif KI, Jawad AK, Al-Saqur IM. The prevalence of hydatid cysts in slaughtered animals in Iraq. Ann. Trop. Med. Parasitol. 1980; 74: 185-7.

Arda B, Yamazhan T, Demirpolat G. Prevalence of Echinococcus granulosus detected using enzyme immunoassay and abdominal ultrasonography in a group of students staying in a state dormitory in Turkey. Turk. J. Med. Sci. 2009; 39: 791-4.

Siracusano A, Teggi A, Ortona E. Human Cystic Echinococcosis: Old Problems and New Perspectives. Inter. disciplinary Perspect. Infect. Dise. 2009; 10: 1155-7.

Hamid AR. Hydatid disease of the brain: A study of 84 cases between 1986-1992. A thesis submitted to the Iraqi Commission of Medical Specialisation, The Scientific Board of Neurosurgery. 1993; 1-76.

Al-Fatalawei MAA. Epidemiological and biological study of hydatidosis in Al-Qadisia governorate. M.Sc. Thesis, College of Veterinary Medicine, University of Baghdad. Iraq. 2002; 1-70.

Akkaya H, Akkaya B, Gönülcü S. Hydatid disease involving some rare sites in the body. Turkiye Parazitol Derg. 2015;39:78-2.

Wani NA, Kousar TL, Gojwari T, et al. Computed tomography findings in cerebral hydatid disease. Turk Neurosurg. 2011;21:347-51.

Al-Witry SH, Al-Zain T. Hydatid disease in Iraq. Neurochirurgia o suppl.1981; 31.

Al-Mufty KSA. Validity of Serological Tests in the Diagnosis of Hydatidosis. An M.Sc. thesis, parasitology, submitted to the Council of the College of Medicine, University of Duhok, 2012, 1-68.

Senapati SP, Parida, DK, Pattajoshi AS, Gouda AK, Patnaik A. Primary hydatid cyst of brain: Two cases report. Asian J Neurosurg. 2015; 10: 175–6.

K?z?lca Ö, Alta? M, ?enol U, Öztek MA. Hydatid Disease Located in the Cerebellomedullary Cistern. Case Rep Med. 2014; (27):13-65.

Okur A, Ogul H, Sengul G, Karaca L, Nalbantoglu NG, Kantarci M. Magnetic resonance spectroscopy and magnetic resonance imaging findings of the intracerebral alveolar echinococcosis. J Craniofac Surg. 2014;25(4):1352-3.

Khalatbari MR, Brunetti E, Shobeiri E, Moharamzad Y. Calcified Mass on Brain CT in a Teenager with Refractory Seizures. Neuroradiol J. 2014;27(6):691-6.

Köktekir E, Erdem Y, Gökçek C et al. Calcified intracranial hydatid cyst: case report. Turkiye Parazitol Derg. 2011;35:220-3.

Gottstein B. Molecular and immunological diagnosis of Echinococcus. Clin. Microbiol. Rev. 1992; 5: 248-61.

Parija SC. A review of some simple immunoassay in the serodiagnosis of cyst hydatid disease. Acta.Trop. 1998; 70: 17-24.

Ammann RW, Eckert J. Cestodes: Echinococcus. Gastroenterol. Clin North Am. 1996; 25: 655-69.

Kohli A, Gupta RK, Poptani H, Roy R. In vivo proton magnetic resonance spectroscopy in a case of intracranial hydatid cyst. Neurology. 1995; 45:562–4.

Arana IR. Echinococcus Infection of the nervous system. In: Vinken PJ, Bruyn GW, editors. Hand Book of Clinical Neurology, Part III. Amsterdam: Elsevier/North Holland Biomedical Press; 1978. pp. 175–208.

Al Zain TJ, Al-Witry SH, Khalili HM, Aboud SH, Al Zain FT Jr. Multiple intracranial hydatidosis. Acta Neurochir (Wien). 2002; 144:1179-85.

Saenz de SPB, Cazaña JL, Cobo J, Serrano CL, Quiralte J, Contreras J, et al. Anaphylactic shock by rupture of hepatic hydatid cyst. Follow-up by specific IgE serum antibodies. Allergy. 1992; 47:568–70.

Senyuz OF, Yesildag E, Celayir S. Albendazole therapy in the treatment of hydatid liver disease. Surg Today. 2001; 31:487–91.

Abu-Eshy SA. Some rare presentations of hydatid cyst (Echinococcus granulosus) J R Coll Surg Edinb. 1998; 43:347–52.

Mushtaque M, Mir M, Malik A, Arif S, Khanday S, Dar R. Atypical Localisations of Hydatid Disease: Experience from a Single Institute. Niger J Surg. 2012; 18: 2–7.

Palaivelu C. Laparoscopic management of hydatid cysts of liver Art of laparoscopic surgery- Textbook and Atlas. Jaypee Publishers; 2007; pp. 757–83.

Mushtaque M, Malik A, Malik R. Hydatid cyst of the gall bladder: A rare location. Eastern Journal of Medicine. 2011; 16:83–6.

Saimot AG. Medical treatment of liver hydatidosis. World J Surg. 2001; 25:15–20.

Downloads

Published

2023-12-05

How to Cite

Al-Rawi, W. W., & Al-Rawi, F. W. . (2023). Cerebral Hydatid Disease Patients Admitted to Duhok City Hospitals: Management and Outcome. AMJ (Advanced Medical Journal) , 8(2), 23-30. https://doi.org/10.56056/amj.2023.214

Issue

Section

Articles