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Artykuły w czasopismach na temat „Pulmonary hydatid disease”

Autor: Grafiati

Data publikacji: 3 czerwca 2025

Data aktualizacji: 31 lipca 2025

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1

Kaur Sandhu, Azmat, Pavneet Kaur Selhi, and Ruchita Tyagi. "Pulmonary hydatid disease." IP Journal of Diagnostic Pathology and Oncology 4, no. 4 (2019): 338–41. http://dx.doi.org/10.18231/j.jdpo.2019.069.

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Kaskar, Ameya, Varun Shetty, and Devi Shetty. "Chronic pulmonary thromboembolism due to intracardiac and pulmonary hydatidosis." Asian Cardiovascular and Thoracic Annals 28, no. 9 (2020): 610–12. http://dx.doi.org/10.1177/0218492320957918.

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Hydatid disease remains a problem in endemic areas. The combination of both intracardiac and pulmonary hydatid disease in association with chronic pulmonary thromboembolism is a rare presentation. We report a case of a 14-year-old girl with hydatid disease of the lungs, right ventricle, and pulmonary arteries, presenting as chronic pulmonary thromboembolism. She underwent surgery for wedge resection of the pulmonary hydatid in the right lower lobe, removal of the right ventricular hydatid (under cardiopulmonary bypass), and pulmonary endarterectomy (under total circulatory arrest). Her postope

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3

Samargandy, Shaza A. "Complicated Pulmonary Hydatid Disease:." Saudi Journal of Internal Medicine 5, no. 1 (2015): 47–52. http://dx.doi.org/10.32790/sjim.2015.5.1.8.

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Hydatid disease is a zoonotic parasitic infection that is more prevalent in the developing world and among pastoral communities. This report discusses this case along with a brief review of the pulmonary echinococcosis literature. This is a case report of a pulmonary hydatid disease in a young man whose disease course was complicated by spontaneous pneumothorax and empyema. His chest computerized tomography scan revealed the characteristic (Water Lily sign) which is pathognomonic for pulmonary hydatidosis. With proper anti-helminthic and antibiotic treatment along with surgical management, the

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4

Alam, Md Tarek, Sadia Saber, Rafa Faaria Alam, and Mohammad Monower Hossain. "Primary Pulmonary Hydatid Disease." Bangladesh Critical Care Journal 6, no. 2 (2018): 105–7. http://dx.doi.org/10.3329/bccj.v6i2.38589.

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Echinococcosis is a parasitic disease endemic in many parts of the world. Liver is the most common affected organ followed by lungs. However, the infestation of the latter is usually secondary to another infected organ system. Symptoms are not specific and can be produced by the mass effect or cyst complications. In the article we are reporting a case of pulmonary echinococcosis in a middle aged male, where the patient presented with symptoms of fever, cough with expectoration, weight loss and dysponea. An extensive work-up showed no other foci of infestation, hence final diagnosis was done ba

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5

Farhan Kadhim Al-Rubaye, Ali. "Complicated Pulmonary Hydatid Disease." University of Thi-Qar Journal Of Medicine 26, no. 2 (2024): 809–21. https://doi.org/10.32792/jmed.v26i2.603.

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Background: Echinococcus is widely distributed parasite through temperate and subtropical region where sheeps are extensively raised. In Iraq, the disease is endemic and is considered to be one of the most serious helminthic diseases in the country. Patients and Methods: 170 surgically treated patients with pulmonary hydrated disease. They were admitted to the thoracic and cardiovascular department at Ibn Al Nafees teaching hospital from the 1st of January 1998 to the first of October 1999. Results: Eighty patients were only presented with different complications, forty-three females and thirt

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6

El Belidi, Abir, Hajar El Ouartassi, Latifa Oukerraj, and Mohamed Cherti. "HYDATID PULMONARY EMBOLISM: AN EXTREMELY RARE COMPLICATION OF HYDATID DISEASE." International Journal of Advanced Research 10, no. 04 (2022): 610–15. http://dx.doi.org/10.21474/ijar01/14591.

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The location of hydatid cysts inside the pulmonary artery is extremely rare. The cause is usually the rupture of intracardiac cysts. Only a few case reports of hydatid pulmonary embolism are reported in the literature.Herein, we describe the clinical case of a young 30-year-old patient, functionally asymptomatic, in whom multiple hydatid pulmonary embolisms were discovered on a CT scan which was done as part of the extension assessment of a hydatid cyst. We will discuss the pathophysiology as well as the management of this case. Recognition of the unique radiologic findings of hydatid cyst emb

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7

Koul, Parvaiz A., Ajaz N. Koul, A. Wahid, and Farhad A. Mir. "CT in Pulmonary Hydatid Disease." Chest 118, no. 6 (2000): 1645–47. http://dx.doi.org/10.1378/chest.118.6.1645.

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8

Beacom, Sabrina, Priya Nand, Parampreet Singh, and Anil Harrison. "Isolated pulmonary hydatid cyst." BMJ Case Reports 16, no. 8 (2023): e254876. http://dx.doi.org/10.1136/bcr-2023-254876.

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Echinococcosis is primarily a disease of developing nations with poor medical infrastructure, where cohabitation with domesticated animals is common. These conditions, in conjunction with the inherent chronicity of the disease, lead to low rates of diagnosis and high morbidity. Robust surveillance is not readily available in communities with the highest disease burden.WHO classifications assist in diagnostic and treatment endeavours especially in countries where this disease is not commonly encountered. However, the understanding of the pathophysiology of echinococcosis and optimal treatment a

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9

Zaimi, Soukaina, Habib Bellamlih, and Ittimade Nassar. "Hydatid pulmonary embolism: An exceptional complication of hydatid disease." Radiology Case Reports 15, no. 5 (2020): 545–47. http://dx.doi.org/10.1016/j.radcr.2020.01.015.

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10

Amchich, Y., H. El ouzzani, A. Rhorfi, and A. Abid. "Pulmonary Hydatidosis and Hydatid Pulmonary Embolism." Scholars Journal of Medical Case Reports 12, no. 04 (2024): 407–9. http://dx.doi.org/10.36347/sjmcr.2024.v12i04.006.

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We present an extremely rare case of a old man 52 answith hydatid pulmonary embolism caused by a direct invasion of the pulmonary artery by a hydatid cyst. Even if it is a benign parasitic disease, it can lead to serious complications such as arterial, systemic, or multivisceral dissemination or being responsible for an anaphylactic shock. Because of the clinical polymorphism, the diagnosis can be delayed. Therefore, A chest CT angiography is the gold standard for the positive diagnosis.

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11

Laldayal, Deepthi. "Unusual Coexistence of Pulmonary Tuberculosis and Hydatid Disease." Journal of Postgraduate Medicine, Education and Research 52, no. 1 (2018): 36–39. http://dx.doi.org/10.5005/jp-journals-10028-1273.

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ABSTRACT Tuberculosis and hydatidosis are both infectious diseases commonly involving the pulmonary system and exhibiting a wide spectrum of clinical manifestations of varying severity. The simultaneous occurrence of pulmonary tuberculosis and hydatid disease is extremely rare, reported sporadically in the literature. We herein report two cases where this rare coexistence was proven after radiological features aroused suspicion. The first patient was a young female with a short history of fever and cough. She had miliary mottling and a cystic lesion on imaging. Second patient was an elderly la

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12

Gadea, I., G. Ayala, M. T. Diago, A. Cuñat, and J. García de Lomas. "Immunological Diagnosis of Human Cystic Echinococcosis: Utility of Discriminant Analysis Applied to the Enzyme-Linked Immunoelectrotransfer Blot." Clinical Diagnostic Laboratory Immunology 6, no. 4 (1999): 504–8. http://dx.doi.org/10.1128/cdli.6.4.504-508.1999.

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ABSTRACT An enzyme-linked immunoelectrotransfer blot for the diagnosis of human hydatid disease was performed, and the different antibody responses were analyzed by a discriminant analysis. This multivariate technique gave us, first, a selection of the most important responses against Echinococcus granulosus infection and, second, a procedure for the classification of patients into two groups: patients with hydatid disease and patients without a history of hydatid disease. This method was applied to 67 patients, 25 with active hydatid cysts (24 hepatic and 1 pulmonary) and 42 without a history

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13

S, Kanugula, Pasam Y, and Baddula D. "A rare association of brucellosis and pulmonary hydatid cyst in a patient with human immunodeficiency virus." Journal of Medical and Scientific Research 11, no. 2 (2023): 145–48. http://dx.doi.org/10.17727/jmsr.2023/11-27.

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Background: Hydatid disease, or cystic echinococcosis, is a parasitic infection caused by a tapeworm. Pulmonary hydatid infection is the second common manifestation of hydatid disease. We present a patient who was diagnosed with recurrent hydatid cyst in lung and later diagnosed with brucellosis, which is a highly contagious zoonotic disease. Case presentation: A 47-years-old male was diagnosed with pulmonary hydatid disease after a computed tomography (CT) chest-plain was done. As the patient had high intermittent fever for 4 months which could not be explained by an intact cyst in the follow

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14

Laatoub, H1* Kanté MC1 Moatassim Billah N2 Bourkadi JE1 and Marc K1. "Hydatid Pulmonary Embolism: A Case Report." Mega Journal of Case Reports 7, no. 9 (2024): 2001–8. https://doi.org/10.5281/zenodo.13710956.

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<strong>Abstract</strong> Hydatid disease is a parasitic infection common in certain regions, particularly in Mediterranean countries, where it primarily affects the liver and lungs. Hydatid pulmonary embolism (HPE) is a rare and potentially life-threatening complication characterized by the rupture of a hydatid cyst and the release of cystic material into the circulation, it commonly occurs when a hydatid cyst of the right heart or liver through the inferior vena cava or hepatic vein. Although HPE is uncommon, it carries significant morbidity and mortality risks, underscoring the critical nee

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15

Kumar, N., M. Mishra, and A. Singhal. "Pulmonary hydatid cyst - A radiological challenge!" SAARC Journal of Tuberculosis, Lung Diseases and HIV/AIDS 9, no. 1 (2012): 39–42. http://dx.doi.org/10.3126/saarctb.v9i1.6964.

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Hydatid disease is a parasitic infestation caused by Echinococcus granulosus. The resulting large cysts in the lung, a special clinical entity called giant hydatid cysts, is rare. Our case involves a middle-aged man who presented to us with vague chest complaints. Chest X-ray revealed a large cavity with an airfl uid level in the right hemithorax, which brought to the mind a constellation of differential diagnoses. A diagnosis of hydatid cyst was made intraoperatively. This case report provides evidence that radiological findings may be misleading and cause a diagnostic delay in such cases. SA

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16

Manouchehr Aghajanzadeh, Ali Alavi Foumani, Azita Tangestaninejad, et al. "Report a rare case of pulmonary hydatid cyst which present as massive pleural effusion." GSC Advanced Research and Reviews 14, no. 1 (2023): 088–94. http://dx.doi.org/10.30574/gscarr.2023.14.1.0012.

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Common cause of massive pleural effusions (MPE) are malignancy, tuberculosis and parapneumonic effusion,. Parasitic infections are very rare causes of (MPE). Echinococcosis or hydatid disease is a major public health problem in poor hygienic country in the world. The liver is most common organ involved and lungs are the secound most frequently involved organs. Pulmonary hydatid cyst appears to be more common in younger individuals. Echinococcus granulosus is most common type and Echinococcus multilocularis hydatid cyst causes alveolar hydatid cyst, which accounts for <5%of all cases of hyda

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17

Manouchehr, Aghajanzadeh, Alavi Foumani Ali, Tangestaninejad Azita, et al. "Report a rare case of pulmonary hydatid cyst which present as massive pleural effusion." GSC Advanced Research and Reviews 14, no. 1 (2023): 088–94. https://doi.org/10.5281/zenodo.7678475.

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Common cause of massive pleural effusions (MPE) are malignancy, tuberculosis and parapneumonic effusion,. Parasitic infections are very rare causes of (MPE). Echinococcosis or hydatid disease is a major public health problem in poor hygienic country in the world. The liver is most common organ involved and lungs are the secound most frequently involved organs. Pulmonary hydatid cyst appears to be more common in younger individuals. Echinococcus granulosus is most common type and <em>Echinococcus multilocularis</em> hydatid cyst causes alveolar hydatid cyst, which accounts for <5%o

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18

Marathe, Anant Prabhakar, Mayur Tadvi, and Vaidehi J. Mehta. "Empyema and haemothorax due to ruptured pulmonary hydatid cyst- A rare presentation." IP International Journal of Medical Microbiology and Tropical Diseases 9, no. 2 (2023): 126–28. http://dx.doi.org/10.18231/j.ijmmtd.2023.024.

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Hydatidosis is a parasitic infection caused by Echinococcus granulosus (Dog Tape-worm). India is endemic for hydatid disease. The lung is the second most frequently affected organ by hydatid cysts after the liver. Hydatid cysts are mostly seen in the right lower lobe of the lung. We report an unusual presentation of ruptured pulmonary hydatid cyst as empyema and haemothorax in a 24-year-old boy who presented with dyspnoea on exertion with right-sided chest pain. Pleural fluid was suggestive of empyema. The pleural fluid examination revealed plenty of neutrophils and the presence of hooklets of

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19

Nicoalae, Dogotari, Ambros Igor, Negru Virginia, and Babuci Stanislav. "Diagnostic errors in pulmonary hydatid cyst complicated by spontaneous rupture in the bronchus: clinical case presentation." International Journal of Research in Medical Sciences 11, no. 7 (2023): 2678–81. http://dx.doi.org/10.18203/2320-6012.ijrms20232119.

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Diagnosis and treatment of a pulmonary hydatid cyst complicated by rupture are difficult, especially in cases of late presentation. In this context, the authors report a case of spontaneous rupture of a large pulmonary hydatid cyst diagnosed in a patient 12 years old who was directed to our institution with the preventive diagnosis of a right lung abscess rather late and successfully treated by surgery. The authors conclude that the disease was initially clinically misdiagnosed as a respiratory infection, then a lung abscess, the radiological examination being avoided at the initial stages of

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20

Ekinci, Gülbanu Horzum, Murat Kavas, Osman Hacıömeroğlu, Esra Akkütük Öngel, Ayşe Ersev, and Adnan Yılmaz. "Pulmonary Hydatid Disease Mimicking Lung Cancer." Respiratory Case Reports 4, no. 1 (2015): 60–63. http://dx.doi.org/10.5505/respircase.2015.04909.

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21

Kervancioĝlu, R., M. Bayram, and L. Elbeyli. "CT Findings in Pulmonary Hydatid Disease." Acta Radiologica 40, no. 5 (1999): 510–14. http://dx.doi.org/10.3109/02841859909175576.

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Saksouk, Faysal A., Meheddin H. Fahl, and Ghassan K. Rizk. "Computed Tomography of Pulmonary Hydatid Disease." Journal of Computer Assisted Tomography 10, no. 2 (1986): 226–32. http://dx.doi.org/10.1097/00004728-198603000-00011.

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Kumar, M., D. Raghavendra, K. Mishra, V. Suri, and S. Kumari. "Pulmonary hydatid disease and serpent sign." QJM: An International Journal of Medicine 112, no. 2 (2018): 143. http://dx.doi.org/10.1093/qjmed/hcy208.

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Gouliamos, Athanasios D., Angelos Kalovidouris, John Papailiou, Labros Vlahos, and Constantine Papavasiliou. "CT Appearance of Pulmonary Hydatid Disease." Chest 100, no. 6 (1991): 1578–81. http://dx.doi.org/10.1378/chest.100.6.1578.

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Sokouti, Mohsen, Samad E. J. Golzari, Servet Kayhan, and Babak Sabermarouf. "Recurrence Following Pulmonary Hydatid Disease Surgery." World Journal of Surgery 38, no. 1 (2013): 266. http://dx.doi.org/10.1007/s00268-013-2141-3.

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Baki, Y. N., W. Siner, and F. Khougeer. "Choriocarcinoma presenting as pulmonary hydatid disease." International Journal of Gynecology & Obstetrics 38, no. 4 (1992): 315–18. http://dx.doi.org/10.1016/0020-7292(92)91025-j.

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Prieto, A., A. Diaz, J. Calvo, and L. López-Negrete. "MR imaging of pulmonary hydatid disease." European Journal of Radiology 23, no. 1 (1996): 85–87. http://dx.doi.org/10.1016/0720-048x(95)00722-3.

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Butler, MW, RH Mullan, KE Schaffer, TB Crotty, DA Luke, and SC Donnelly. "Pulmonary cystic hydatid disease in Ireland." Irish Journal of Medical Science 172, no. 4 (2003): 204–5. http://dx.doi.org/10.1007/bf02915291.

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Ozvaran, Mustafa Kursat, Yesim Ersoy, Bahadir Uskul, et al. "Pleural complications of pulmonary hydatid disease." Respirology 9, no. 1 (2004): 115–19. http://dx.doi.org/10.1111/j.1440-1843.2003.00518.x.

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Thula, Stanley Amos, Meryline Ndlovu, and Refiloe Masekela. "The different faces of pulmonary hydatid disease." South African Respiratory Journal 22, no. 2 (2016): 43. http://dx.doi.org/10.7196/sarj.2016.v22i2.74.

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<p style="margin: 0cm 0cm 8pt 36pt;"> </p><p align="left">Hydatid disease is responsible for causing cystic disease. In children, it classically involves the liver, lung and brain but can involve almost any organ or numerous organs simultaneously. e lung is the most common target organ in children, while in adults hepatic involvement is more common. We present three case reports of children who presented with hydatid disease with varying clinical manifestations of pulmonary hydatidosis and complications, and their related management.</p><p style="margin: 0cm 0cm 8pt

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Al-Hakkak, Samer Makki Mohamed, Ashraf Sami Muhammad, and Saad Ab-Razq Mijbas. "Splenic-preserving surgery in hydatid spleen: a single institutional experience." Journal of Medicine and Life 15, no. 1 (2022): 15–19. http://dx.doi.org/10.25122/jml-2021-0221.

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Though hydatid disease affects many organs in the human body, splenic hydatid accounts for approximately 0.8-4% of all human echinococcosis cases. Up to recently, splenectomy was the preferred surgery for hydatid spleen. Since 1980, conservative options to treat such a disease have become more and more prevalent. Our study aimed to assess our experience in open splenic preservative surgery for splenic hydatid in a single institutional center. Our retrospective research included ten patients with splenic hydatid operated between August 2013 and January 2018 at our medical center. The spleen was

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Errihani, Majdouline, Aya Sobhi, Kawtar Hassani, Sanaa Benbria, and Driss El Kabbaj. "Association of Membranous Nephropathy and Tubulointerstitial Nephritis with Hepatic Hydatidosis: Case Report." SAS Journal of Medicine 10, no. 05 (2024): 471–75. http://dx.doi.org/10.36347/sasjm.2024.v10i05.041.

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Hydatid disease is an anthropozoonosis due to development of Echinococcus larva in the human host. This parasitic infection causes rarely a renal damage, that’s why only a few cases of glomerular or tubulointerstitial nephropathies linked to hepatic or pulmonary hydatic cysts, have been reported during the last three decades. We report a singular case of membranous nephropathy and tubulointerstitial nephritis associated with a hepatic hydatidosis.

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Balta, Cenk. "Uniportal-Single Incision Thoracoscopic Access for Pulmonary Hydatid Cysts." Current Respiratory Medicine Reviews 15, no. 1 (2019): 39–44. http://dx.doi.org/10.2174/1573398x15666190508090653.

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Objective: Pulmonary hydatid cyst is caused by Echinococcus Species and has high prevalence in low and middle income countries. Surgery remains the gold standard method for this parasitic pulmonary disease. Here, we report 20 cases of pulmonary hydatid cysts that underwent minimally invasive videothoracoscopic surgery. Methodology: All the patients who underwent minimally invasive complete thoracoscopic removal of pulmonary hydatid cysts in our clinic, which were recorded in the hospital database had been extracted. Clinical properties and complications of the surgeries were analyzed retrospec

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Manouchehr, Aghajanzadeh, Alavi Foumani Ali, Tangestaninejad Azita, et al. "Presentation, diagnosis, management and outcome of complicated hydatid cyst of the lung." GSC Advanced Research and Reviews 18, no. 2 (2024): 362–73. https://doi.org/10.5281/zenodo.11216544.

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<strong>Introduction:</strong> Introduction: The complicated hydatid cyst of the lung is defined as any cyst ruptured in the bronchi tree or in the pleural cavity, infected, and rarely in the pericardial cavity. The aim of this study was to evaluate the problems of complicated pulmonary hydatid cyst, including presentation, diagnosis choice of surgical methods. and complication of delay in surgical treatment of pulmonary hydatid cysts. <strong>Methods: </strong>Between 2016 and 2021, 192 operations operated for pulmonary hydatid cysts, 42 of these patients were complicated hydatid cy

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Amirian, Armin, Bizhan Ziaian, Amirhossein Erfani, Reza Shahriarirad, and Keivan Ranjbar. "Successful Management of a Huge Pulmonary Hydatid Cyst with Lung-Preserving Surgery." Case Reports in Surgery 2020 (March 17, 2020): 1–4. http://dx.doi.org/10.1155/2020/9526406.

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The lung is the second most commonly involved organ in humans by hydatid disease. Management of large pulmonary hydatid cysts is a great challenge for thoracic surgeons. Lung resections should be considered the last choice for huge pulmonary hydatid cysts when the lung expansion is not optimal after cyst removal. Here, we present a case of huge lung hydatid cyst involving the entire right lower lobe which was successfully managed by lung-preserving surgery in which the postoperative course showed gradual resolution of the involved lobe during a one-year follow-up.

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Lone, Yasir Ahmad, Santosh Singh, Shikha Tyagi, Aisha Naaz, and Brijesh Kumar Tiwari. "Clinical Pattern of Pediatric Hydatid Disease." Journal of Indian Association of Pediatric Surgeons 29, no. 2 (2024): 122–28. http://dx.doi.org/10.4103/jiaps.jiaps_186_23.

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ABSTRACT Context: Literature regarding hydatid disease in children is sparse. Aims: To highlight the peculiarities in the clinical pattern of pediatric hydatid disease (PHD). Settings and Design/Materials and Methods: Data were collected retrospectively from all children aged <18 years who presented to our tertiary care institute from July 2021 to June 2023 with hydatid disease involving any organ. Statistical Analysis Used: Simple statistical analysis involving sums, means, averages, and percentages. Results: Four of the 10 cases (40%) involved the lung, while only 2 (20%) involved the liv

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Jbara, O., H. Safieddine, M. Labied, et al. "Mediastino-Pulmonary Hydatidosis Complicated by False Aneurysm." SAS Journal of Medicine 9, no. 05 (2023): 408–10. http://dx.doi.org/10.36347/sasjm.2023.v09i05.003.

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Multiple thoracic hydatidosis with vascular involvement is exceptional but has a very poor prognosis. The authors report the observation of a 32 year old patient, hospitalized for cough and recurrent hemoptysis. Chest radiography showed "balloon-like" images. Chest CT scan showed cystic formations in the lungs and a false aortic aneurysm. Hydatid serology was strongly positive. A medical treatment with albendazole was prescribed, but the patient died of massive hemoptysis before surgical resection of the false aneurysm, which was recommended under extracorporeal circulation. An analysis of our

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Meshram, Rajkumar M., Vishal S. Gajimwar, Kavitha G., and Sadullah Saqulain Khwaja. "Pulmonary hydatid cyst in children." International Journal of Contemporary Pediatrics 7, no. 5 (2020): 1171. http://dx.doi.org/10.18203/2349-3291.ijcp20201664.

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Hydatidosis is a zoonotic parasitic disease with global existence caused by tapeworm of family Taeniidae and genus Echinococcus. It is transmitted by feco oral route or direct contact with dogs. A 7-year-old female was admitted with cough, fever, chest pain and history of contact with dog. Chest radiography showed round to oval mass with air fluid level while ultrasonography of thorax was suggestive of a large cystic lesion in right mid zone with dense moving echo and multiple hyper echoic foci with connected artifacts without calcification. Computerized tomography showed large cystic lesion c

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Aydin, Yunus, Orhan Barlas, Coşkun Yolaş, et al. "Alveolar hydatid disease of the brain." Journal of Neurosurgery 65, no. 1 (1986): 115–19. http://dx.doi.org/10.3171/jns.1986.65.1.0115.

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✓ Four cases of alveolar hydatid disease of the brain encountered within 27 months in eastern Turkey are reported. All of the patients were male farmers who presented with signs of cerebral tumor. Two of the patients were shown to harbor hepatic lesions and one of them had pulmonary metastases. The cerebral lesions were removed in toto and neurological recovery was obtained in all four patients. A review of the literature revealed only five previously reported cases treated surgically. It is concluded that cerebral Echinococcus multilocularis lesions are amenable to surgery, and that their rem

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Fifer, H. M., P. L. Chiodini, S. B. Lucas, and J. S. Brown. "Invasive aspergillosis associated with pulmonary hydatid disease." Travel Medicine and Infectious Disease 10, no. 5-6 (2012): 272–74. http://dx.doi.org/10.1016/j.tmaid.2012.07.001.

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Mawhorter, Steven, Barbara Temeck, Richard Chang, Harvey Pass, and Theodore Nash. "Nonsurgical Therapy for Pulmonary Hydatid Cyst Disease." Chest 112, no. 5 (1997): 1432–36. http://dx.doi.org/10.1378/chest.112.5.1432.

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Liu, Zhengyu, Bin Yang, Haijun He, et al. "Computed tomography diagnosis of pulmonary hydatid disease." Radiology of Infectious Diseases 9, no. 3 (2022): 104. http://dx.doi.org/10.4103/rid.rid_25_22.

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Ceberut, Kadri. "Pulmonary hydatid cyst disease: a retrospective study." Current Thoracic Surgery 8, no. 1 (2023): 32. http://dx.doi.org/10.26663/cts.2023.005.

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Menon V., Haripriya. "RUPTURED PULMONARY HYDATID CYST PRESENTING AS PLEURAL EFFUSION IN A THIRD TRIMESTER PREGNANT WOMAN." International Journal of Advanced Research 12, no. 12 (2024): 1097–100. https://doi.org/10.21474/ijar01/20117.

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Background: Hydatid disease is a zoonotic disease caused by infection with Echinococcus granulosus .Pulmonary hydatid cyst often becomes symptomatic after cyst rupture in the pleural cavity or bronchus.Pulmonary hydatid cyst may be misdiagnosed and therefore patients may receive inappropriate treatment.In this case, a 27-year-old full term pregnant female presented with sudden onset dyspnea and hypoxia. Upon further evaluation, it was found to be a ruptured hydatid. Case Report: A 27 year old full term(36 weeks) pregnant patient was admitted with sudden onset of dyspnea,fever and hypoxia(SpO2-

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Behrad, Mohammad Sayed, Sayed Hussain Mosawi, and Sayed Hussain Amiri. "Extra-Pulmonary Hydatid Cyst from Afghanistan: A Case Report." Afghanistan Journal of Infectious Diseases 3, no. 1 (2025): 101–4. https://doi.org/10.60141/ajid.93.

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Hydatid cysts, caused by the larval stages of Echinococcus tapeworms, are a significant parasitic infection primarily affecting the liver and lungs. This case report presents a rare instance of an extrapulmonary hydatid cyst located in the pleural of a 45-year-old housewife female patient from Afghanistan. The patient exhibited symptoms of chest pain, headaches, dizziness, and a dry cough over three years. Diagnostic CT imaging revealed a mass in the right thoracic region. Following thorough surgical preparation, a right posterior-lateral thoracotomy was performed, leading to the excision of t

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Aldahmashi, Mohammed, Mohamed Alassal, Ibrahim Kasb, and Hany Elrakhawy. "Conservative Surgical Management for Pulmonary Hydatid Cyst: Analysis and Outcome of 148 Cases." Canadian Respiratory Journal 2016 (2016): 1–6. http://dx.doi.org/10.1155/2016/8473070.

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Background. Hydatid cyst (HC) disease is endemic in many developing countries, like Yemen, Egypt, and Saudi Arabia, especially in the rural regions. The disease has a variable clinical courses and even might be asymptomatic for many years.Objectives. In giant and large pulmonary hydatid cysts, pulmonary resection is the usual method of surgical treatment. In this study, we aimed to evaluate the lung conservative surgery in treatment of cases with giant and large hydatid lung cysts, as an effective method of management.Patients and Methods. Between January 2009 and August 2014, a total of 148 p

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Jamil Ur Rehman, Tahir Raza, Saddam Hussain, Hamdan Khan, and Muhammad Abid Khan. "Outcome of Open Enucleation with Capitonnage for Hydatid Lung Disease in Children." Indus Journal of Bioscience Research 3, no. 5 (2025): 713–16. https://doi.org/10.70749/ijbr.v3i5.1469.

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Introduction: Hydatid cystic disease remains an endemic surgical problem in many part of world including Indian subcontinent. Most commonly involved organs are the liver (60%-80%) and the lung (10%-40%) but it can involve any part of body. Surgery is preferable treatment of pulmonary hydatid among various surgical procedure open enucleation with capitonnage is preferred procedure. Objectives: To determine outcome of open enucleation with capitonnage for hydatid lung disease in children in term of postoperative complications and length hospital stay. Materials and Methods: This descriptive stud

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Banihashemi, Seyed Hesamaddin, Seyedeh Hanan Banihashemi, Ahmadreza Karimi, Seyed Hosein Asadi Yousefabad, Younes Askari, and Manouchehr Aghajanzadeh. "Investigating Pulmonary Hydatidosis: A Narrative Review." Hormozgan Medical Journal 28, no. 2 (2024): 59–66. http://dx.doi.org/10.34172/hmj.8203.

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Context: Pulmonary hydatidosis (PH) is a zoonotic illness caused by infection with the Echinococcus tapeworm species. About 20% of the infected individuals have lung involvement in this disease, which is epidemiologically secondary to liver disease. Evidence Acquisition: A comprehensive literature search was performed via the Scopus, PubMed, Cochrane Library, and Google Scholar databases. Search terms were "pulmonary hydatidosis," "lung hydatidosis," "Pulmonary echinococcosis," "lung echinococcosis," "Pulmonary hydatid cyst," and "Lung hydatid cyst." The search period of 1980 to 2022 was chose

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Talukder, Md Saiful Hoque, Subash Chandra Mandal, Md Shafiqul Islam, et al. "Cardiac Hydatid Cyst: First Ever Documented Case in Bangladesh." Bangladesh Heart Journal 32, no. 2 (2018): 125–29. http://dx.doi.org/10.3329/bhj.v32i2.36100.

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Hydatid cystic disease results from infection with the larval or adult form of the Echinococcus Granulosus(tapeworm). Cardiac involvement is seen in 0.5% to 2% of patients withhydatid disease and involvement of the right atrium(RA), main pulmonary artery(MPA) and right pulmonary artery(RPA) are very rare.In this case a 22-yr-old farmer woman from Raigong, Sirajgong, Bangladesh presented to the ShahidZiaur Rahman Medical College hospital, Bogra with the complaints of breathlessness for 10 months; haemoptysis and chest pain for last 3 months.CT scan of the chest showed cystic lesion on right hil

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Gottstein, Bruno, and Jürg Reichen. "Hydatid lung disease (echinococcosis/hydatidosis)." Clinics in Chest Medicine 23, no. 2 (2002): 397–408. http://dx.doi.org/10.1016/s0272-5231(02)00007-2.

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