Case Report of a large family with hyperparathyroidism- jaw tumor syndrome (HPT-JT) and a deletion of the third exon of CDC73

2019 ◽  
Author(s):  
Collen Lauriane Le ◽  
Sara Barraud ◽  
Odou Marie Francoise ◽  
Marta Spodenkiewicz ◽  
Antoine Braconnier ◽  
...  
Keyword(s):  
Case Report ◽  
Large Family ◽  
The Third

A Case of Sparganosis Mansoni Manifesting as Creeping Eruption-The Third Case Report in Okinawa-

2012 ◽  
Vol 74 (1) ◽  
pp. 31-36 ◽  
Author(s):  
Naoko NAKASONE ◽  
Eriko UEHARA ◽  
Masataka KORENAGA ◽  
Sayaka YAMAGUCHI ◽  
Kenzo TAKAHASHI ◽  
...  
Keyword(s):  
Case Report ◽  
The Third ◽  
Creeping Eruption

scholarly journals Atypical Chordoid Glioma of the Third Ventricle: A Case Report

2015 ◽  
Vol 04 (02) ◽  
pp. 124-127
Author(s):  
R. Mittal ◽  
Amitesh Dubey ◽  
S. Singhvi ◽  
Manash Bora
Keyword(s):  
Case Report ◽  
Third Ventricle ◽  
The Third ◽  
Chordoid Glioma

Traumatic Dislocation of the Fourth and Fifth Carpo–Metacarpal Joints: A Case Report

1988 ◽  
Vol 13 (2) ◽  
pp. 210-211
Author(s):  
J. O. STORM
Keyword(s):  
Case Report ◽  
X Rays ◽  
The Third ◽  
Traumatic Dislocation

A case of traumatic dislocation of the fourth and fifth carpo-metacarpal joints and fracture of the base of the third metacarpal is presented. It is recommended that lateral X-rays of the hand be taken if dislocation is suspected at this level, as the injury may be missed on standard X-rays.

Primary Non-Hodgkin's Lymphoma Involving the Third Ventricle: A Case Report

2001 ◽  
Vol 44 (4) ◽  
pp. 415
Author(s):  
Hae Jeong Jeong ◽  
Ghi Jai Lee ◽  
Jae Chan Shim ◽  
Young Cho Koh ◽  
Mee Joo ◽  
...  
Keyword(s):  
Case Report ◽  
Hodgkin’S Lymphoma ◽  
Third Ventricle ◽  
Hodgkin's Lymphoma ◽  
The Third ◽  
Non Hodgkin’S Lymphoma ◽  
Non Hodgkin's Lymphoma

scholarly journals Case report: a 5-year-old with new onset nephrotic syndrome in the setting of COVID-19 infection

2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Kelsi M. Morgan ◽  
Peace D. Imani
Keyword(s):  
Nephrotic Syndrome ◽  
Case Report ◽  
Pediatric Patient ◽  
Corticosteroid Therapy ◽  
Clinical Remission ◽  
Laboratory Findings ◽  
Case Presentation ◽  
The Third ◽  
First Case ◽  
New Onset

Abstract Background This is a case report of an asymptomatic SARS-CoV-2 infection associated with new-onset nephrotic syndrome in a pediatric patient. This is the third case of new-onset nephrotic syndrome in children associated with SARS-CoV-2 infection, but is the first case report describing a new-onset nephrotic syndrome presentation in a patient who had asymptomatic COVID-19 infection. Case presentation This is a case of a previously healthy 5 year old female who presented with new-onset nephrotic syndrome in the setting of an asymptomatic COVID-19 infection. She presented with progressive edema, and laboratory findings were significant for proteinuria and hypercholesterolemia. She was treated with albumin, diuretics, and corticosteroid therapy, and achieved clinical remission of her nephrotic syndrome within 3 weeks of treatment. Though she was at risk of hypercoagulability due to her COVID-19 infection and nephrotic syndrome, she was not treated with anticoagulation, and did not develop any thrombotic events. Conclusions Our case report indicates that SARS-CoV-2 infection could be a trigger for nephrotic syndrome, even in the absence of overt COVID-19 symptoms.

scholarly journals Primitive Anorectal Malignant Melanoma: A Rare And Aggressive Localization A Case Report

2020 ◽  
Vol 7 (07) ◽  
pp. 4871-4874
Author(s):  
Amal Hajri ◽  
Abdessamad El Azhary ◽  
Driss Erguibi ◽  
Rachid Boufettal ◽  
Saad Rifki El Jai ◽  
...  
Keyword(s):  
Liver Transplantation ◽  
Case Report ◽  
Malignant Melanoma ◽  
Rare Condition ◽  
University Hospital ◽  
Anorectal Melanoma ◽  
Review Of The Literature ◽  
The Third ◽  
Anorectal Malignant Melanoma ◽  
Digestive Cancers

Primary anorectal malignant melanoma is an extremely rare condition. It appears at the third highest frequency after melanomas of the skin and retina. Its prognosis is dreadful because of the early onset of metastases. The treatment remains essentially surgical. We report an observation of primitive anorectal melanoma, collected at the department of surgery for digestive cancers and liver transplantation of the Ibn Rochd University Hospital of Casablanca, with a review of the literature. In order to analyse the clinical, paraclinical and therapeutic characteristics of primary anorectal melanoma.

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