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Journal articles on the topic 'Intracerebral hydatid cyst'

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1

Thapa, Ashish Jung, Asheesh Tandon, and Alok Agrawal. "Giant Intracerebral Hydatid Cyst in a Boy." Nepal Journal of Neuroscience 17, no. 1 (2020): 44–47. http://dx.doi.org/10.3126/njn.v17i1.28346.

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Giant intra-cerebral hydatid cysts are an extremely rare condition caused by the infestation of larvae of Taenia echinococcus (TE). Humans are infected through the feco-oral route by the ingestion of food and milk, contaminated by dog feces containing the ova of parasite or direct contact with dogs. We report a case of a seventeen-year-old boy with giant right temporo-parieto-occipital hydatid cysts (HC).
 Giant intracerebral hydatid cysts being rare and can at times lead to death, so surgical excision with preoperative consideration and intraoperative rupture prevention is the best manag
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2

Garg, Deepak, Gaurav Jain, and Virendra Sinha. "A Case Report of Primary Brain Hydatid Cyst in a Child." Iranian Journal of Neurosurgery 6, no. 1 (2020): 41–48. http://dx.doi.org/10.32598/irjns.6.1.7.

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Background and Importance: Hydatid cyst is endemic in India, with different clinical presentations according to the site of involvement in the body. However, its occurrence in the brain without the involvement of other body parts is rare. Case Presentation: An eight-year-old female child presented with right-sided limb weakness and slurring of speech. The diagnosis of primary brain hydatid cyst was made with Magnetic Resonance Imaging (MRI) of the brain. The cyst was removed completely, resulting in improved post-operative slurring of speech and limb weakness. Conclusion: In countries where hy
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3

Turgut, Mehmet, Kemal Benli, and Muzaffer Eryilmaz. "Secondary multiple intracranial hydatid cysts caused by intracerebral embolism of cardiac echinococcosis: an exceptional case of hydatidosis." Journal of Neurosurgery 86, no. 4 (1997): 714–18. http://dx.doi.org/10.3171/jns.1997.86.4.0714.

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✓ The authors present an extremely rare case of secondary multiple cerebral echinococcosis caused by presumed intracerebral and arterial embolism of cardiac hydatidosis in a 7-year-old girl. The first manifestations were symptoms of raised intracranial pressure. Unfortunately, before the primary ruptured echinococcosis cyst was detected in the myocardium of the left ventricle, the patient underwent nine operations over an 8-year period for hydatid embolism affecting the brain and the femoral artery and was treated with concurrent mebendazole therapy. The combined therapy would not have been su
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4

Touzani, Soumaya, Brahim Bechri, Toufik Joulali, Mohamed Adnane Berdai, Smael Labib, and Mustapha Harandou. "Intracerebral hydatid cyst: A rare cause of neurosurgical emergency." International Journal of Case Reports and Images 7, no. 11 (2016): 758. http://dx.doi.org/10.5348/ijcri-2016133-cr-10721.

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5

Ketaren, R. J., J. Simca, and V. Hartoyo. "Silent intracerebral hydatid cyst presenting with atypical neurologic deficits." Journal of the Neurological Sciences 405 (October 2019): 131–32. http://dx.doi.org/10.1016/j.jns.2019.10.1016.

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6

Hamrah, Abdul Rahim. "A Rare Case of Multiple Intracerebral Hydatid Cysts in a Pediatric Patient: A Case Report with Emphasis on Surgical Precision." Indiana Journal of Humanities and Social Sciences 6, no. 4 (2025): 10–12. https://doi.org/10.5281/zenodo.15233620.

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<strong>Abstract: </strong>Background: Intracerebral hydatid disease is a rare manifestation of Echinococcus granulosus infection, particularly in pediatric populations. The presence of multiple cerebral cysts poses significant diagnostic and surgical challenges. <strong>Case Presentation:</strong> We report a rare case of multiple intracerebral hydatid cysts in a 7-year-old girl from Faryab Province, Afghanistan, who presented with progressive neurological symptoms, including headache, left-sided weakness, and anisocoria over an eight-month period. MRI revealed multiple well-defined cystic le
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7

Palani, Arun. "Partially calcified giant intracerebral hydatid cyst in a pediatric child." Neurology India 60, no. 2 (2012): 260. http://dx.doi.org/10.4103/0028-3886.96437.

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8

Cindea, Cosmin-Nicodim, Vicentiu Saceleanu, and Adriana Saceleanu. "Intraoperative Rupture of an Intracranial, Extradural Hydatid Cyst: Case Report and Treatment Options." Brain Sciences 11, no. 12 (2021): 1604. http://dx.doi.org/10.3390/brainsci11121604.

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A 23-year-old woman was presented to the Emergency Unit with intracranial hypertension syndrome and blindness in her left eye which had started recently. A cranial native computed tomography scan and a magnetic resonance imaging (MRI) with contrast examinations revealed a giant intracranial cystic lesion, extending into the left frontal lobe, which was compressing the optic chiasm and eroding the internal plate of the left frontal bone. Surgical craniotomy was performed for evacuation and decompression, but during the craniotomy the cyst ruptured. After assessing the degree of erosion of the i
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9

Saleh, SamehM. "Successful surgical management of intracerebral hydatid cyst in children: timing, procedure, and adjuvant treatment." Journal of Medicine in Scientific Research 3, no. 4 (2020): 303. http://dx.doi.org/10.4103/jmisr.jmisr_77_20.

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10

Singounas, E. G., A. S. Leventis, D. E. Sakas, D. M. Hadley, D. A. Lampadarios, and P. C. Karvounis. "Successful Treatment of Intracerebral Hydatid Cysts with Albendazole." Neurosurgery 31, no. 3 (1992): 571???574. http://dx.doi.org/10.1097/00006123-199209000-00022.

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11

Singounas, E. G., A. S. Leventis, D. E. Sakas, D. M. Hadley, D. A. Lampadarios, and P. C. Karvounis. "Successful Treatment of Intracerebral Hydatid Cysts with Albendazole." Neurosurgery 31, no. 3 (1992): 571–74. http://dx.doi.org/10.1227/00006123-199209000-00022.

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12

Sierra, Jorge, Jorge Oviedo, Marcelo Berthier, and Ramon Leiguarda. "Growth rate of secondary hydatid cysts of the brain." Journal of Neurosurgery 62, no. 5 (1985): 781–82. http://dx.doi.org/10.3171/jns.1985.62.5.0781.

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✓ Bilateral intracerebral hydatid cysts developed in a 14-year-old patient after an infarct of presumed embolic origin in the left frontotemporoparietal region. The average rate of growth of these cysts was about 5 cm per year. This suggests that the growth rate is far from uniform and indeed, particularly in young patients, may be much faster than originally estimated.
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13

Bankole, N. D. A., M. Denou, M. C. Sayore, et al. "Intracerebral Calcific Hydatic Cyst Mimicking Calcific Hematoma: A Case Report." Yangtze Medicine 04, no. 01 (2020): 79–83. http://dx.doi.org/10.4236/ym.2020.41008.

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14

Ugˇur, H. C., A. Attar, C. Bagˇdatogˇlu, A. Erdogˇan, and N. Egemen. "Secondary Multiple Intracranial Hydatid Cysts Caused by Intracerebral Embolism of Cardiac Echinococcosis." Acta Neurochirurgica 140, no. 8 (1998): 833–34. http://dx.doi.org/10.1007/s007010050186.

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15

Kadri, Hassan, Mazen Dughly, Raed Abouharb, and Sameer Bakleh. "A rare entity of primary hydatid cyst located between the two laiers of the intracranial dura in a child: a case report." European Journal of Medical Case Reports 8, no. 1 (2024). http://dx.doi.org/10.24911/ejmcr/173-1685692046.

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Background: Hydatid disease is a parasitic infection caused by the tapeworm Echinococcus granulosus. Intracranial hydatid cysts are rare and account for less than 3% of all cases of hydatid disease. Typically, these cysts are found in the intracerebral spaces. However, this study presents an extremely rare intradural hydatid cyst. Case Presentation: This study presents the case of an 8-year-old boy presented with a 3-month history of headache and vomiting without any neurological deficit. Full radiological investigations were performed, and only brain magnetic resonance imaging showed a large
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16

Kadri, Hassan, Mazen Dughly, Raed Abouharb, and Sameer Bakleh. "A rare entity of primary hydatid cyst located between the two laiers of the intracranial dura in a child: A case report." European Journal of Medical Case Reports, 2024, 01–04. http://dx.doi.org/10.24911/ejmcr.173-1685692046.

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ABSTRACT Background: Hydatid disease is a parasitic infection caused by the tapeworm Echinococcus granulosus.Intracranial hydatid cysts are rare and account for less than 3% of all cases of hydatid disease. Typically, these cysts are found in the intracerebral spaces. However, this study presents an extremely rare intradural hydatid cyst. Case presentation: This study presents the case of an 8-year-old boy presented with a 3-month history of headache and vomiting without any neurological deficit. Full radiological investigations were performed, and only a brain magnetic resonance imaging showe
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17

Kadri, Hassan, Mazen Dughly, Raed Abouharb, Sameer Bakleh, and Rostom Mackieh. "A rare entity of primary hydatid cyst located between the two layers of the intracranial dura in a child: a case report." Oxford Medical Case Reports 2023, no. 12 (2023). http://dx.doi.org/10.1093/omcr/omad107.

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Abstract Introduction: Hydatid disease is a parasitic infection caused by the tapeworm Echinococcus granulosus. Intracranial locations are rare and account for less than 3% of all cases. Typically, these cysts are found in the intracerebral spaces. However, this study presents an extremely rare intradural hydatid cyst. To our knowledge no similar case has been previously reported. Case presentation: This study presents the case of an 8-year-old boy presented with a 3-month history of headache and vomiting without any neurological deficit. Full radiological investigations were performed, the br
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18

Singh, Rohan Kumar, Prerna Anup Patwa, Gaurav Vedprakash Mishra, Rajasbala Pradeep Dhande, Shivali Vaibhav Kashikar, and Bhavik Sunit Unadkat. "An unusual case report on intracranial hydatid cyst with intraventricular extension." Egyptian Journal of Radiology and Nuclear Medicine 53, no. 1 (2022). http://dx.doi.org/10.1186/s43055-022-00727-x.

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Abstract Background We report an interesting case of a primary isolated intraventricular and intracranial hydatid cyst in 20-year-old female that mimicked bleeding cystic tumor presenting as intraventricular hemorrhage with hydrocephalus. Case presentation Patient presented with headache and giddiness for 1 month. On magnetic resonance imaging, there was multiloculated multi-cystic lesion in left lateral ventricle and adjacent left periventricular deep white matter. Lesion was causing compression of the body of the left lateral ventricle with temporal horn dilatation and midline shift of 17–18
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19

Hafedh, Anwar N., Awfa A. Aktham, Zahraa F. Al-Sharshahi, et al. "Primary multiple cerebral hydatid disease in a young patient with surgically-treated intracerebral haemorrhage." Romanian Neurosurgery, March 9, 2021, 71–74. http://dx.doi.org/10.33962/roneuro-2021-011.

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Introduction: Cerebral hydatid disease (CHD) is rare and the multiple-cystic variety is even rarer. In this paper, we report a case of multiple CHD and explore a possible link with a preceding spontaneous intracerebral haemorrhage (ICH). &#x0D; Case presentation: A 27-year old gentleman with a history of surgically-evacuated, spontaneous ICH presented with severe headache, left-sided weakness - Medical Research Council (MRC) grade II - and recurrent tonic-clonic seizures, while on a full dose of anti-epileptic medication. Brain magnetic resonance imaging (MRI) scans showed multiple intra-axial
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20

Hilmani, Said, Adil Maati, and Abdessamad El Azhari. "Combined Intracerebral and Cranial epidural Hydatid Cysts: Case Report." International Journal of Radiology & Radiation Therapy 2, no. 2 (2017). http://dx.doi.org/10.15406/ijrrt.2017.02.00021.

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