scholarly journals Giant Cerebral Hydatid Cyst; A Rare Case Report

2020 ◽  
Author(s):  
Babak Ganjeifar ◽  
Majid Ghafouri ◽  
Azar Shokri ◽  
Farhad Rahbarian Yazdi ◽  
Seyed Ahmad Hashemi
Keyword(s):  
Abdominal Pain ◽  
Case Report ◽  
Hydatid Cyst ◽  
Rare Case ◽  
Cerebral Hydatid Cyst ◽  
Rare Case Report ◽  
History Of

Here we describe a 13- year old patient with the presentation of fever and abdominal pain. He had a history of 2 years headache and seizure. In MRI, a primary cerebral hydatid cyst was evident. The diagnosis of hydatid cyst should beconsidered in children with mentioned characters in endemic regions.

scholarly journals Pelvic Hydatid Cyst with Hydroureteronephrosis: A Rare Case Report

2021 ◽  
Vol 2021 ◽  
pp. 1-4
Author(s):  
Amir Mohammad Salehi ◽  
Hossain Salehi ◽  
Ensiyeh Jenabi
Keyword(s):  
Abdominal Pain ◽  
Case Report ◽  
Hydatid Cyst ◽  
Rare Case ◽  
Parasitic Disease ◽  
Body Parts ◽  
Antibody Index ◽  
Rare Case Report ◽  
Primary Hydatid Cyst ◽  
Cystic Masses

Hydatid cyst is a parasitic disease caused by Echinococcus granulosus or Echinococcus multilocularis. Humans are accidentally infected with the parasite. The cyst is usually found in the liver and lungs and rarely occurs in other body parts. The present article describes a rare case of pelvic hydatid cyst in a young man who presented with nausea, vomiting, and right abdominal pain. Two large cystic masses were discovered during a CT scan in the patient’s pelvic region, resulting in right urinary tract hydroureteronephrosis. Additionally, the antibody index was used to confirm the presence of a primary hydatid cyst.

scholarly journals Unusual localizations of hydatid cysts: a rare case report from Syria

2020 ◽  
Vol 2020 (10) ◽  
Author(s):  
Zain Douba ◽  
Judy A Sinno ◽  
Haya Jawish ◽  
Nour Hakim ◽  
Abdullah Mouselli ◽  
...  
Keyword(s):  
Abdominal Pain ◽  
Case Report ◽  
South America ◽  
Rare Case ◽  
Eastern Mediterranean ◽  
Left Lung ◽  
Hydatid Cysts ◽  
Rare Case Report ◽  
History Of ◽  
The Right

Abstract Hydatid disease (HD) is an infection with the metacestode stage of the tapeworm Echinococcus. It is commonly seen in South America, The Middle East, Eastern Mediterranean, Africa and China. Hydatid cysts usually affect the liver followed by the lungs. Involvement in other organs has been reported. However, in the majority of the cases, cysts are localized in one organ or one region. We report a rare case of a 36-year-old woman who presented to the hospital in Syria with long-standing history of non-specific abdominal pain. Computerized tomography showed several hydatid cysts in the liver, spleen, left lung, mediastinum (adjacent to the aortic arch), both breasts and above the right gluteal muscles.

scholarly journals Giant Cerebral Hydatid Cyst: A Rare Case Report

2021 ◽  
Vol 9 (3) ◽  
pp. 1774-1778
Author(s):  
Babak Ganjeifar ◽  
Majid Ghafouri ◽  
Azar Shokri ◽  
Farhad Rahbarian Yazdi ◽  
Seyed Ahmad Hashemi
Keyword(s):  
Case Report ◽  
Hydatid Cyst ◽  
Rare Case ◽  
Cerebral Hydatid Cyst ◽  
Rare Case Report

Bilateral Lung and Liver Hydatid Cyst with Massive Hydropneumothorax: A Rare Case Report in Kuwait

2021 ◽  
Vol 04 (04) ◽  
Author(s):  
Ahmad E Al-Mulla ◽  
Derar Al Shehab ◽  
Essa AlGhunaim ◽  
Ehab Saad Imam ◽  
Hamad F Alsanea
Keyword(s):  
Case Report ◽  
Hydatid Cyst ◽  
Rare Case ◽  
Liver Hydatid Cyst ◽  
Rare Case Report ◽  
Bilateral Lung

scholarly journals Primary ovarian hydatid cyst in a postmenopausal woman: A rare case report

2020 ◽  
Vol 68 ◽  
pp. 221-223 ◽  
Author(s):  
Taxiarchis Katsamagkas ◽  
Ioannis Tsakiridis ◽  
Dimitrios Evaggelinos ◽  
Paraskevi Skafida ◽  
Themistoklis Dagklis ◽  
...  
Keyword(s):  
Case Report ◽  
Postmenopausal Woman ◽  
Hydatid Cyst ◽  
Rare Case ◽  
Rare Case Report

scholarly journals Non-painful severe variant form of eruptive lingual papillitis: A case report and literature review

2021 ◽  
Vol 13 (2) ◽  
Author(s):  
Manal Ahmed Halwani
Keyword(s):  
Emergency Department ◽  
Case Report ◽  
Literature Review ◽  
Oral Hygiene ◽  
Rare Case ◽  
Dorsal Surface ◽  
Variant Form ◽  
Girl Child ◽  
Rare Case Report ◽  
History Of

Eruptive lingual papillitis is a common benign disorder manifested by inflammation of fungiform papillae on the dorsolateral surface of the tongue. Several variants of lingual papillitis have been reported since 1997, most or all of them with painful erythematous papules. Here we report a case of 6 years old girl child with non-painful severe variant form of eruptive lingual papillitis presented to the emergency department. The entire dorsal surface of the tongue was surfaced by 2-3mm by multiple erythematous papules and some with a white or yellowish colour. The papules were excessively inflamed, pigmented, aggregated, and crusted. The cause was idiopathic which resolved within ten days. The parent and patient were reassured with advice to practice oral hygiene. This is a rare case report describing non-painful lingual papillitis without a history of any prior episodes.

scholarly journals A ruptured cornual pregnancy successfully managed in a patient with a history of oophorectomy and salpingectomy: A rare case report

2021 ◽  
Vol 9 (10) ◽  
Author(s):  
Marah Mansour ◽  
Amr Hamza ◽  
AlHomam AlMarzook ◽  
Ilda moafak kanbour ◽  
Tamim Alsuliman ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Cornual Pregnancy ◽  
Rare Case Report ◽  
History Of

The fatal cholera like diarrhoea in coronavirus disease 2019(COVID-19)- a rare case report in toddler

2020 ◽  
Vol 11 (SPL1) ◽  
pp. 1894-1897
Author(s):  
Varsha Gajbhiye ◽  
Shubhangi Patil (Ganvir) ◽  
Sarika Gaikwad
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Digestive System ◽  
Gastrointestinal Symptoms ◽  
Female Child ◽  
Multiple Organ ◽  
Mild Case ◽  
Severe Dehydration ◽  
Rare Case Report ◽  
History Of

A 14-month female child came with complain of cholera like watery loose stool 10-12 times and vomiting 6-7 times, 24 hrs before admission. She was in severe dehydration, hypotension, unconscious with no recorded fever during her stay in hospital and no history of contact with COVID-19. Patient was COVID-19 positive Dehydration and hypotension was corrected, metabolic acidosis continued and eventually patient succumb due to multiple organ failure. This case report should arouse us to suspect COVID infection in every acute Gastroenteritis child who may not have any common symptoms as seen in COVID patient, also who have no history of significant contact with COVID positive patient in family. Some people with COVID-19 develop gastrointestinal symptoms either alone or with respiratory symptoms. Recently, researchers at Stanford University found that a third of patients they studied with a mild case of COVID-19 had symptoms affecting the digestive system. Another recent study Trusted Source published by researchers in Beijing found that anywhere from 3 to 79 percent of people with COVID-19 develop gastrointestinal symptoms.

Rare case of perforated appendicitis presenting as persistent perineal discharge following laparoscopic abdominoperinal excision of rectum (APER)

2021 ◽  
Vol 14 (1) ◽  
pp. e236312
Author(s):  
Tanmoy Mukherjee ◽  
Shantata Jayant Kudchadkar ◽  
Jayesh Sagar ◽  
Shashank Gurjar
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Perforated Appendicitis ◽  
Perineal Wound ◽  
Abdominoperineal Excision ◽  
Major Surgery ◽  
Salvage Procedure ◽  
Uncommon Presentation ◽  
Rare Case Report ◽  
History Of

Abdominoperineal excision of rectum (APER) is one of the widely used surgical procedures to treat low rectal cancer, benign conditions like Crohn’s proctitis with anal involvement and as a salvage procedure for anal cancer. Perineal wound infection is a well-recognised complication following such major surgery. Occurrence of appendicitis in a few weeks’ time following such a major surgery is uncommon. However, here we present a rare case report of perforated appendicitis presenting as persistent perineal discharge in an elderly man, following laparoscopic APER for a low rectal tumour. To our knowledge, this is the first time such a rare clinical presentation of appendicitis is reported in the history of medical literature. Through this case report, we aim to highlight the importance of considering such an uncommon presentation in patients with perineal discharge, following APER.

Bizarre extensive erythematous plaques on the abdomen

2018 ◽  
Vol 49 (1) ◽  
pp. 39-42
Author(s):  
Sidharth Tandon ◽  
Surabhi Sinha ◽  
Jasmeet Singh
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rare Case Report ◽  
History Of ◽  
Erythematous Plaques

We present a rare case report of a 28-year-old man with a five-month history of bizarre extensive erythematous plaques on the abdomen extending in a dermatomal fashion to the left upper back.

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