Results 71 to 80 of about 21,807 (192)

Severe Nasofacial Necrosis From Capnocytophaga canimorsus: A Case Report of Disease and Reconstruction

Eye &ENT Research, Volume 3, Issue 1, Page 33-36, March 2026.
Armon Hadian, Jason Azzi, Benjamin Taylor   +2 more
wiley   +1 more source

Thrombotic Thrombocytopenic Purpura, Moschcowitz Syndrome [PDF]

, 2001
The authors present a case of a 16-year-old boy, who was referred to the hospital due to thrombocytopenia, anemia, proteinuria and hyperbilirubinemia. Based on the clinical picture and the laboratory data, thrombotic thrombocytopenic purpura (TTP) was ...
Czinyéri, Judit, Sasvári, Ildikó, Kovács, Gábor, Garami, Miklós, Müller, Judit   +4 more
core   +1 more source

Thrombosis in Brothers With Protein S Deficiency: Case Series

Clinical Case Reports, Volume 13, Issue 9, September 2025.
ABSTRACT Hereditary protein S deficiency is a rare thrombophilia that increases the risk of venous thromboembolism (VTE), including thrombosis in unusual sites. Early diagnosis, familial screening, and long‐term anticoagulation are essential for preventing complications and improving outcomes.
Abate Bane Shewaye, Seifu Kebede, Amsalework Daniel, Kaleb Assefa Berhane, Asteraye Tsige Minyilshewa, Besufikad Girma Kebede   +5 more
wiley   +1 more source

Genotypic and phenotypic character of Chinese neonates with congenital protein C deficiency: a case report and literature review

Thrombosis Journal, 2019
Background Our objective was to study the phenotype of and molecular genetic mechanisms underlying congenital protein C (PC) deficiency in Chinese neonates.
Xiaoying Li, Xiaoyan Li, Xiao Li, Yuanhua Zhuang, Lili Kang, Xiuli Ju   +5 more
doaj   +1 more source

A case of purpura fulminans secondary to transient protein C deficiency as a complication of chickenpox infection

The Turkish Journal of Pediatrics, 2002
Purpura fulminans is a rare but dramatic disease which occurs most commonly during or after an infection. It is characterized by extensive involvement of the skin and extremities and involvement of visceral organs.
Cengiz Canpolat, Mustafa Bakir
doaj  

Púrpura fulminans asociada a un caso probable de síndrome de choque tóxico estafilocócico en el Hospital III Cayetano Heredia, Piura, Perú

Acta Médica Peruana, 2008
Introducción: púrpura fulminans por infección estafilocócica es una asociación poco común que se viene observado con mayor frecuencia en los últimos años. Caso clínico: se presenta aquí el caso de una paciente de 20 años que desarrolló púrpura fulminans
Daniel G. La Rosa Zambrano
doaj  

Acral Purpura Fulminans With Erythrocyte-Associated Streptococcus pneumoniae: A Case Report

Annals of Internal Medicine: Clinical Cases
A patient presented with acral purpura fulminans caused by Streptococcus pneumoniae septicemia. With antibiotics and intensive care, he survived but required amputations of both hands and feet due to ischemic necrosis.
Donald L. Granger, Jeannine Pembroke, Todd R. Gordon   +2 more
doaj   +1 more source

Purpura Fulminans with Consumptive Coagulopathy in Gram Negative Sepsis

, 2002
purpura fulminans with consumptive coagulopathy (DIC) in gram negative ...
Lawrence, Christine
core  

Fatal purpura fulminans and Waterhouse-Friderichsen syndrome from fulminant Streptococcus pneumoniae sepsis in an asplenic young adult [PDF]

, 2016
Asplenic patients are at increased risk for sepsis and fulminant infection. Sepsis in these patients is typically secondary to encapsulated bacteria, with Streptococcus pneumoniae being the most frequent pathogen.
Baden, Rachel, Kirby, James E., Hale, Andrew J., LaSalvia, Mary, Kimball, Allison   +4 more
core   +1 more source

Purpura fulminans secondary to toxic shock syndrome induced by Group A Streptococcal bacteremia in an adult patient [PDF]

Purpura fulminans is a rare life-threatening presentation of disseminated intravascular congestion that presents with widespread purpura and skin necrosis secondary to considerable tissue thrombosis.
Hartmann, Bredesen, Kemper, Kortni, Blaise, Brittany   +2 more
core   +1 more source