scholarly journals A Rare Case Report- An Incidental Finding of Isolated Unilocular Splenic Hydatid Cyst

2021 ◽  
pp. 259-265
Author(s):  
Shubham Satyaprakash Gupta ◽  
Sangita Jogdand Shinde ◽  
Raju K. Shinde ◽  
Shweta Pandey
Keyword(s):  
Case Report ◽  
Hydatid Cyst ◽  
Rare Case ◽  
Unusual Case ◽  
Incidental Finding ◽  
Abnormal Uterine Bleeding ◽  
Rare Presentation ◽  
Rare Case Report ◽  
Total Splenectomy ◽  
Splenic Hydatid Cyst

Splenic Hydatid Cyst is a very rare presentation with less than 5% of total incidences of Cystic Echinococcosis. It is usually due to spread of cysts from other regions leading to secondaries. Primary isolated splenic hydatid cyst without involvement of any other organs is even rarer. We report an unusual case of a female who presented as Abnormal Uterine Bleeding (AUB) with an incidental finding of Isolated Splenic Hydatid Cyst with absence of involvement of any other organ. Patient underwent laparotomy and total splenectomy was done. This case report targets to report a rare case of incidental finding of isolated unilocular hydatid cyst of spleen and describes its management.

scholarly journals Mobile caecum as a content in recurrent incisional hernia an incidental finding: A rare case report

2021 ◽  
Vol 81 ◽  
pp. 105672
Author(s):  
Chinniahnapalaya Pandurangaiah Hariprasad ◽  
Rohit Gupta ◽  
Anil Kumar ◽  
Deepak Kumar Jha ◽  
Shiv Kishor ◽  
...  
Keyword(s):  
Case Report ◽  
Incisional Hernia ◽  
Rare Case ◽  
Incidental Finding ◽  
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 Bilateral Sturge Weber Syndrome- a rare case report

2013 ◽  
Vol 5 (1) ◽  
pp. 129-132 ◽  
Author(s):  
P Singh ◽  
S Singh
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Unusual Case ◽  
The Other ◽  
Advanced Stage ◽  
Weber Syndrome ◽  
Rare Case Report ◽  
The Face ◽  
Bilateral Condition ◽  
Sturge Weber Syndrome

Background: Sturge-Weber syndrome is a rare congenital neuro- oculo- cutaneous disorder. Objective: To report a very rare unusual case of bilateral manifestation of Sturge Weber syndrome. Case: We report an unusual case of a 17-year-old female with advanced stage of bilateral glaucoma associated with facial nevus extending to the other half of the face as well and bilateral intracranial calcification. Conclusion: Sturge -Weber syndrome can manifest as a bilateral condition. Nepal J Ophthalmol 2013; 5(9):129-132 DOI: http://dx.doi.org/10.3126/nepjoph.v5i1.7841

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 Syphilitic Balanitis of Follmann, A Rare Case Report

2021 ◽  
Vol 19 (1) ◽  
pp. 71-73
Author(s):  
Pooja Agarwal ◽  
Ashish Jagati ◽  
Priyanka Vadher ◽  
Malay Chaudhary
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rare Presentation ◽  
Heterosexual Male ◽  
Primary Syphilis ◽  
Rare Case Report

Syphilitic balanitis of Follmann is a rare presentation of primary syphilis. It can occur before or after the appearance of primary chancre and some time without any associated primary chancre. We are reporting a case of syphilitic balanitis of Follmann, in a 23 years old heterosexual male, who presented with balanitis associated with single indurated lesion over coronal sulcus and few superficial ulcers over prepuce.

scholarly journals Psoriasiform Mycosis Fungoides Involving the Face- A Rare Case Report

2021 ◽  
pp. 94-99
Author(s):  
N. R. Vignesh ◽  
Shreya Srinivasan ◽  
G. Sukanya ◽  
S. Arun Karthikeyan
Keyword(s):  
Case Report ◽  
Mycosis Fungoides ◽  
Rare Case ◽  
Cell Lymphoma ◽  
Punch Biopsy ◽  
Cutaneous T Cell Lymphoma ◽  
Rare Presentation ◽  
Rare Case Report ◽  
Atypical Cells ◽  
The Face

Mycosis fungoides is represented as the most common epidermotropic cutaneous T-cell lymphoma, which is mainly characterized by the proliferation of atypical cells within the epidermis. We report a rare presentation of mycosis fungoides in a 60-year-old male presenting with chronic psoriasiform plaque involving the face. Punch biopsy of the lesion from the forehead was taken for routine histological examination and immunohistochemical stains. Results of biopsy and immunohistochemical findings were consistent with mycosis fungoides and diagnosed as psoriasiform presentation of mycosis fungoides involving the face.

scholarly journals Low-Grade Endometrial Stromal Sarcoma in a 22-Year-Old Maiden Female: A Rare Case Report from Syria

2021 ◽  
Vol 2021 ◽  
pp. 1-4
Author(s):  
Lana Nseir ◽  
Georget Mansour ◽  
Junior Makhoul ◽  
Luna Skaf ◽  
Mohammad Ziad Dahhan ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Treatment Plan ◽  
Endometrial Stromal Sarcoma ◽  
Abnormal Uterine Bleeding ◽  
Low Grade ◽  
Stromal Sarcoma ◽  
Rapid Enlargement ◽  
Rare Case Report ◽  
Immunohistochemical Studies

Endometrial stromal sarcoma (ESS) is a rare and challenging type of endometrial tumor, constituting only about 0.2% of all uterine malignancies and occurring in women 42–58 years of age. ESS is usually misdiagnosed as leiomyoma. They both have nonspecific symptoms, which makes the diagnosis of ESS difficult to achieve. As the ESS is infrequently encountered, optimal management is quite debatable. Here, we report a rare case of a 22-year-old Syrian female who presented with abnormal uterine bleeding; the preoperative diagnosis suggested leiomyoma while histopathological and immunohistochemical studies confirmed the diagnosis of LG-ESS stage IIA. Therefore, the treatment plan was shifted from a conservative myomectomy to a total hysterectomy with both adnexa. The aim of this case report is to draw attention to this uncommon tumor at young age of patients as well as to have awareness of the necessity to suspect this diagnosis especially with the presentation of rapid enlargement of uterine leiomyoma.

scholarly journals Isolated Bilateral Zygomatic Complex and Arch Fracture: A Rare Case Report

2010 ◽  
Vol 3 (4) ◽  
pp. 185-187 ◽  
Author(s):  
Manikandhan Ramanathan ◽  
Mathew Pynumootil Cherian
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Unusual Case ◽  
Rare Case Report

This is an unusual case of isolated bilateral zygomatic complex and arch fracture, which is extremely rare. The literature has no such report of a case.

scholarly journals Ruptured primary uterine serosal hydatid cyst: a rare case report

2005 ◽  
Vol 2 (1) ◽  
pp. 25-26 ◽  
Author(s):  
Arshad H. Malik ◽  
Saima Bashir ◽  
Assar Ahmad Rather
Keyword(s):  
Case Report ◽  
Hydatid Cyst ◽  
Rare Case ◽  
Rare Case Report
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