scholarly journals An unusual manifestation of hydatid disease: A case in a 20-year old male patient

IDCases ◽  
2022 ◽  
Vol 27 ◽  
pp. e01359
Author(s):  
Jonathan Minagogo Hart ◽  
Fiker Eshetu ◽  
Seyoum Kassa
Author(s):  
Veda Murthy Reddy Pogula ◽  
Ershad Hussain Galeti ◽  
Bhargava Reddy Kanchiv ◽  
Ifrah Ahmad ◽  
Ayesha Galeti

Hydatid disease is caused by Echinococcus granulosus, which causes rare isolated presentation in the kidneys, and is estimated to be about 2-4% of all cases. We herein present a case of a 45-year-old symptomatic male patient with a large primary hydatid cyst in the left kidney that was treated successfully by laparoscopic left nephrectomy.


2019 ◽  
Vol 9 (1) ◽  
pp. 30-32
Author(s):  
Punyapratap Singh ◽  
Somshankar Pandey ◽  
Vrishbhan Ahirwar

Primary Muscle involvement of hydatid disease is a rare entity. Radiological diagnosis can be difficult at times as it mimics soft tissue tumor. Multiple imaging studies are available to detect it preoperatively. We hereby report an in a male patient with hydatid disease of adductor group of muscles of right thigh diagnosed on ultrasound followed by MRI and confirmed on surgery and histopathological examination.


2016 ◽  
Vol 2016 ◽  
pp. 1-5
Author(s):  
Ibtisam Musallam Aljohani ◽  
Khalefa Ali Alghofaily ◽  
Sebastian R. McWilliams ◽  
Mnahi Bin Saeedan

A tailgut cyst is a rare developmental lesion and usually is located in the retrorectal or presacral space. Extrahepatic hydatid disease has been reported in several locations including the pelvis and it often poses a diagnostic challenge. There are very few reported cases of primary perineal hydatid cysts. We present the multimodality imaging findings of a tailgut cyst and concurrent perineal hydatid disease in a 32-year-old male patient.


2010 ◽  
Vol 4 (04) ◽  
pp. 256-258 ◽  
Author(s):  
Saulat H Fatimi ◽  
Nida Sajjad ◽  
Marium Muzaffar ◽  
Hashim M Hanif

Patients with echinococcus infection are mostly asymptomatic. The documented rates of simple pneumothorax in patients with pulmonary hydatidosis ranged from 2.4% - 6.2%. We report a case of a forty-year-old male patient who was referred to our hospital for management of recurrent pneumothorax. A video assisted thoracoscope (VATS) was first introduced which showed a large amount of pus in the pleural cavity and a perforated hydatid cyst. The VATS was converted to an open thoracotomy and decortication was done with removal of the ruptured hydatid. The patient made an unremarkable recovery and was discharged after one week with empyema tubes. The empyema tubes were gradually removed over a period of six weeks. An extraordinary number of management options for pulmonary hydatid disease have been offered. This case report highlights surgical treatment as the management opti


Blood ◽  
2020 ◽  
Vol 136 (Supplement 1) ◽  
pp. 8-8
Author(s):  
Cory Mellon ◽  
Salma Ferouz ◽  
Tariq Mubarak ◽  
Isoken Koko

Unusual manifestation of hemolytic anemia due to COVID-19 in an otherwise healthy older male patient without any significant co-morbidity. The presentation consisted of features typical of hemolytic anemia with other causes excluded, signifying a viral etiology of this disease process that has not yet been reported. Other known etiologies of hemolytic anemia were ruled out with extensive history and laboratory data, implying the SARS-COV2 virus was the only determining factor. Disclosures No relevant conflicts of interest to declare.


Author(s):  
Yigit Duzkoylu ◽  
◽  
Ali Imran Kucuk ◽  

Hydatid disease, mostly caused by Echinococcus granulosus, is a common parasitic infestation of the liver. In this type of infectious disease, humans are an intermediate host. Although most common sites are liver (70%) and lungs (25%), this parasitic tapeworm can be seen at any region of the body. Intraperitoneal cysts are usually secondary to the rupture of primary cysts, but primary hydatid cysts of the mesentery are very rare (%2). Herein, we aimed to report a giant primary hydatid cyst in a male patient, treated surgically without any complications.


2021 ◽  
Vol 14 (7) ◽  
pp. e244034
Author(s):  
Vaibhav Kumar Varshney ◽  
Bharti Varshney ◽  
Sudeep Khera ◽  
Binit Sureka

Primary adenocarcinoma of the fourth portion of the duodenum (D-IV) is reported infrequently than other parts of the duodenum. Its diagnosis is often late because of non-specific symptoms and signs. We encountered a 48-year-old male patient who was diagnosed as duodeno-duodenal intussusception, underwent segmental duodenal resection with duodenojejunal anastomosis and confirmed as adenocarcinoma of D-IV. He received adjuvant chemotherapy and is doing well at 1 year of follow-up. This report describes about the rare case of isolated adenocarcinoma of the D-IV presented as intussusception which is never reported before and successfully treated by segmental resection of the duodenum and jejunum.


2015 ◽  
Vol 2015 (apr22 1) ◽  
pp. bcr2015209387-bcr2015209387 ◽  
Author(s):  
K. P. Makaritsis ◽  
C. Liaskos ◽  
G. Papadamou ◽  
G. N. Dalekos

2019 ◽  
Vol 28 (3) ◽  
pp. 548-552
Author(s):  
Andro Košec ◽  
Ivan Kruljac ◽  
Jakov Ajduk

Objective Current recommendations for cochlear hydrops treatment include systemic glucocorticoids and diuretics. Cochlear cells express dopamine receptors, although their role is unknown in the pathophysiology of cochlear hydrops. Case Description We report the case of remission of recurrent right-sided cochlear hydrops in a young male patient treated with bromocriptine due to pituitary macroprolactinoma. Transient improvement was observed after oral steroid and diuretic treatment, but cochlear hydrops recurred until the dose of bromocriptine was increased to 10 mg daily. Conclusion Bromocriptine may stimulate dopamine receptors in cochlear cells with potential therapeutic role in patients with cochlear hydrops. There are no widely accepted and effective treatments for endolymphatic hydrops, and identifying potential new and efficacious therapeutics is of high relevance.


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