Congenital Agenesis of Both Vertebro-Basilar Artery-A Rare Case Report

2021 ◽  
Vol 11 (Number 2) ◽  
pp. 68-71
Author(s):  
Tahmina Siddika ◽  
Ashraful Hasib ◽  
Avijith Bhattacharjee ◽  
Naziur Rahman ◽  
M H Khan Pavel ◽  
...  
Keyword(s):  
Case Report ◽  
Intraventricular Hemorrhage ◽  
Rare Case ◽  
Rare Condition ◽  
Cerebral Angiogram ◽  
Case Presentation ◽  
Rare Case Report ◽  
Basilar Arteries ◽  
Congenital Agenesis ◽  
The Brain

Vertebral and basilar arteries are the major blood suppliers of the brain. They supply nearly one-third of the brain. Congenital absence of these arteries is a rare condition. Usually, this condition presents with stroke like presentation. This is a case presentation of a 40-year-old lady who was diagnosed as congenital agenesis of vertebra-basilar arteries. This lady was presented with intraventricular hemorrhage. Subsequently the diagnosis was made by cerebral angiogram.

scholarly journals Fetus papyraceus: a rare case report

2020 ◽  
Vol 7 (1) ◽  
pp. 113-116
Author(s):  
Namita Sindan ◽  
Adheesh Bhandari ◽  
Snigdha Rai ◽  
Devi Gurung
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Fetal Death ◽  
Rare Condition ◽  
Positive Outcome ◽  
Uterine Wall ◽  
Anatomical Location ◽  
Multiple Gestations ◽  
Gynecology And Obstetrics ◽  
Rare Case Report

Fetus papyraceus is a rare condition of a mummified and compressed fetus occurring in multiple gestations where one fetus dies in utero and is merged between the uterine wall and the membranes of living fetus. The blood vessels of the placenta of the two fetuses anastomose with each other, a third cycle occurs, causing fetal death (fetal transfer syndrome). Ultrasonography may identify the Fetus papyraceus, but is not always promising due to anatomical location. Cautious supervision is important during pregnancy for its positive outcome. We report a case of fetus papyraceus in Department of Gynecology and Obstetrics, Paropakar Maternity and Women’s Hospital, Kathmandu, Nepal.

A rare case report of neonatal iliopsoas abscess presenting as swelling of left hip

2020 ◽  
pp. 1-6
Author(s):  
Maimoona Saeed ◽  
Iqtada Haider Shirazi
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Clinical Presentation ◽  
Psoas Abscess ◽  
Rare Condition ◽  
Medical Sciences ◽  
Rare Case Report ◽  
Key Words Abscess ◽  
Systemic Antibiotics ◽  
Bluish Discoloration

Abstract We report the case of a 12 days old baby boy who presented with swelling and bluish discoloration on his left hip at Pakistan Institute of Medical Sciences in November 2018. Ultrasound (USS) was useful in making the diagnosis of a neonatal psoas abscess. He was treated with extraperitoneal drainage and with systemic antibiotics. The clinical presentation and diagnosis, treatment of this rare condition and brief literature review is given in this case report. Key Words: Abscess, Iliopsoas, Neonate, Staphylococcus aureus, Extraperitoneal Drainage. Continuous....

scholarly journals Recurrent endobronchial fibro-epithelial polyposis in a 73-year-old woman

2021 ◽  
Vol 7 (2) ◽  
pp. e14-e14
Author(s):  
Ramin Sami ◽  
Mina Nickpour ◽  
Noushin Afshar Moghaddam
Keyword(s):  
Case Report ◽  
Oral Cavity ◽  
Rare Case ◽  
Benign Tumor ◽  
Main Bronchus ◽  
Rare Condition ◽  
Genitourinary Tract ◽  
Fibroepithelial Polyp ◽  
Interventional Bronchoscopy ◽  
Case Presentation

Introduction: Fibroepithelial polyp (FEP) is a benign tumor that is presented frequently in some of the organs like oral cavity, skin, colon and genitourinary tract, but in airway is rare. Case Presentation: We present a rare case in this paper, with recurrent bronchial FEP that was near completely obstructed right main bronchus that we managed her successfully with interventional bronchoscopy. In this case report we describe this rare condition. Conclusion: Airway FEP is uncommon benign tumor that may obstruct airways and rarely may be recurrent like our case.

scholarly journals Benign Pleural Multicystic Mesothelioma: A Rare Case Report

2021 ◽  
Author(s):  
Alireza Rezvani ◽  
SeyedehMaryam Pishva ◽  
Amirhossein Erfani ◽  
Ahmad Monabati ◽  
Bizhan Ziaian ◽  
...  
Keyword(s):  
Case Report ◽  
Chronic Cough ◽  
Rare Case ◽  
Pleural Mesothelioma ◽  
Case Presentation ◽  
Rare Case Report ◽  
History Of ◽  
The Right ◽  
Lateral Thoracotomy ◽  
Pleural Involvement

Abstract Background: Fewer than 200 benign multicystic peritoneal mesothelioma cases were reported worldwide till 2017, while its pleural involvement has rarely been reported. Case presentation: We report a 70-year-old man who presented with three months history of chronic cough. Surgical resection was performed, and the pathology confirmed benign multicystic pleural mesothelioma. The patient underwent right lateral thoracotomy, wedges resection of the right upper lobe, and parietal pleurectomy and was discharged with an uneventful postop course.Conclusion: Based on published literature to date, this is the second reported case of pleural involvement of this disease.

scholarly journals Urinary Bladder Cavernous Hemangioma in a 3-year-old: A rare case report.

2021 ◽  
Author(s):  
Charles Odongo ◽  
raymond atwine ◽  
Martin Situma ◽  
ambrose okello ◽  
eugene ogwang ◽  
...  
Keyword(s):  
Case Report ◽  
Urinary Bladder ◽  
Cavernous Hemangioma ◽  
Rare Case ◽  
Embryonal Rhabdomyosarcoma ◽  
Bladder Tumors ◽  
Case Presentation ◽  
Rare Case Report

Introduction: Cavernous hemangioma accounts for 0.6% of bladder tumors. We present a rare case Case Presentation: A 3-year-old girl presented with intravaginal swelling, dysuria, and hematuria. She received 26 cycles of VAC for embryonal rhabdomyosarcoma. Histopathology confirmed CH. Conclusion: CH should be considered in the differentials of childhood genitourinary masses.

scholarly journals Idiopathic Haemolacria: A Rare Case Report

2019 ◽  
Vol 20 (2) ◽  
pp. 106-108
Author(s):  
Goutam Kumar Acherjya ◽  
Mohammad Ali ◽  
Keya Tarafder ◽  
Mostofa Kamal Chowdhury ◽  
Md Abdus Salam ◽  
...  
Keyword(s):  
Case Report ◽  
Malignant Melanoma ◽  
Medical Practice ◽  
Rare Case ◽  
Epstein Barr Virus ◽  
Rare Condition ◽  
Thrombocytopenic Purpura ◽  
Barr Virus ◽  
Rare Case Report ◽  
Epstein Barr

Crying with bloody tear, called haemolacria is a very rare condition in medical practice. There are many conditions such as idiopathic thrombocytopenic purpura, trauma (accidental or induced), factors deficiencies, infections (Epstein Barr virus or bacterial), tumours (malignant melanoma or haemangioma), conjunctival telangiectasia, Rendu-Oslar-Weber disease related to haemolacria. But idiopathic haemolacria may occur in some cases. In our case report, a 17-year-old girl presented with idiopathic bilateral haemolacria and gum bleeding associated with pseudoseizure and psychogenic hyperventilation who was treated and well responded to adequate counselling and Amitriptyline. J MEDICINE JUL 2019; 20 (2) : 106-108

scholarly journals Actinomycotic lacrimal canaliculitis: a rare case report

2019 ◽  
Vol 6 (3) ◽  
pp. 973
Author(s):  
Humaira Bashir ◽  
Asifa Nazir
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Opportunistic Infections ◽  
Rare Condition ◽  
Commensal Bacteria ◽  
Epithelial Lining ◽  
Gram Positive ◽  
Anaerobic Organism ◽  
Rare Case Report

Actinomyces israelii is a gram-positive anaerobic organism commonly associated with canaliculitis in adults. Actinomyces are normal commensal bacteria in humans and primarily cause opportunistic infections during immunosuppressive state or when loss of continuity of epithelial lining in mucosa occurs. Lacrimal canaliculitis is a relatively rare condition and is undiagnosed for long periods of time. Being a relatively rare condition, it is commonly overlooked and undiagnosed for long periods of time. Primary chronic canaliculitis is an uncommon problem and Actinomycosis may form in up to 2% of all lacrimal disease. Here present study reports a case of lacrimal canaliculitis caused by Actinomyces israelii.

scholarly journals Odontogenic Fibromyxoma of Maxilla: A Rare Case Report

2015 ◽  
Vol 8 (2) ◽  
pp. 84-88
Author(s):  
Chandra Kant ◽  
Virendra Kumar Prajapati ◽  
Vishwambhar Singh ◽  
Krishna Murari Tiwari
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Posterior Part ◽  
Rare Condition ◽  
Conventional Radiography ◽  
En Bloc Resection ◽  
Bloc Resection ◽  
En Bloc ◽  
Rare Case Report ◽  
Rare Benign Tumor

ABSTRACT Odontogenic fibromyxoma, a myxoma with abundant collagen fibers, is a rare benign tumor of jaw which mostly affects posterior part of mandible. It is ectomesenchymal in origin and probably arises from connective tissue of dental follicle or papilla. Commonly occurs in 2nd or 3rd decade with slight female predilection. Radiological investigations, such as conventional radiography, computed tomography (CT) scan or magnetic resonance imaging (MRI) can be used to differentiate it from other odontogenic tumors like ameloblastoma. Management is surgical by enucleation and curettage or by en bloc resection and segmental maxillectomy. Follow-up of patient is must for at least 2 years to diagnose any recurrence. In this article, we present fibromyxoma of maxilla which is a very rare site for occurrence of fibromyxoma and this relatively rare condition has been discussed in light of recent information from literature with a case report. How to cite this article Kant C, Prajapati VK, Singh V, Tiwari KM. Odontogenic Fibromyxoma of Maxilla: A Rare Case Report. Clin Rhinol An Int J 2015;8(2):84-88.

scholarly journals Myxoid liposarcoma with metastasis to the pancreas: a rare case report and review of the literature

2020 ◽  
Author(s):  
Ankang Wang ◽  
Peng Cong ◽  
Zhenxing He ◽  
Yueyu Qu ◽  
Tao Hu ◽  
...  
Keyword(s):  
Case Report ◽  
Gastrointestinal Bleeding ◽  
Rare Case ◽  
Radical Surgery ◽  
Myxoid Liposarcoma ◽  
Review Of The Literature ◽  
Case Presentation ◽  
Complete Surgical Resection ◽  
Rare Case Report ◽  
Rare Malignancy

Abstract BackgroundMetastasis of the pancreas to myxoid liposarcoma is very rare.Case presentationWe report a 43-year-old woman who underwent radical surgery for myxoid liposarcoma (MLPS) of the sigmoid colon 9 years earlier and for liposarcoma of the neck 7 years earlier. The lesion later metastasized to the pancreas, and we performed pancreaticoduodenectomy, which was pathologically confirmed as myxoid liposarcoma. Unfortunately, the patient died a year later from unexplained gastrointestinal bleeding.ConclusionsMyxoid liposarcoma is a very rare malignancy that carries a risk of invasion to the pancreas, and complete surgical resection is the best chance for clinical treatment.

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