scholarly journals Hemophagocytic Syndrome, an Uncommon Complication of Microscopic Polyangitis: A Case Report From Senegal

2015 ◽  
Vol 7 (6) ◽  
Author(s):  
Mouhamadou Moustapha Cisse ◽  
Daher Abdoul Karim Omar ◽  
Jean De Dieu Nzambaza ◽  
Sidy Ba ◽  
Awa Cheikh Ndao ◽  
...  
Keyword(s):  
Case Report ◽  
Hemophagocytic Syndrome ◽  
Microscopic Polyangitis ◽  
Uncommon Complication

scholarly journals Multiorgan failure due to hemophagocytic syndrome: A case report

Cases Journal ◽  
2008 ◽  
Vol 1 (1) ◽  
Author(s):  
Juan Mayordomo-Colunga ◽  
Corsino Rey ◽  
Soledad González ◽  
Andrés Concha
Keyword(s):  
Case Report ◽  
Hemophagocytic Syndrome ◽  
Multiorgan Failure

scholarly journals Common operation, uncommon complication. Bleeding from superior haemorrhoidal artery after minimally invasive procedure for hemorrhoids – a case report

2019 ◽  
Vol 39 (1) ◽  
pp. 70-73 ◽  
Author(s):  
Janavikula Sankaran Rajkumar ◽  
Aluru Jayakrishna Reddy ◽  
Ravikumar Radhakrishnan ◽  
Anirudh Rajkumar ◽  
Syed Akbar ◽  
...  
Keyword(s):  
Case Report ◽  
Minimally Invasive ◽  
Invasive Procedure ◽  
Minimally Invasive Procedure ◽  
Common Operation ◽  
Uncommon Complication

scholarly journals Inflammatory Pseudotumor of the Liver Complicated by Lung Necrosis and Pleural Empyema: A Case Report

2011 ◽  
Vol 2011 ◽  
pp. 1-3
Author(s):  
Klaus Steinbrück ◽  
Marcelo Enne ◽  
Reinaldo Fernandes ◽  
Jose M. Martinho ◽  
Lúcio F. Pacheco-Moreira
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Inflammatory Pseudotumor ◽  
Liver Tumors ◽  
Rare Condition ◽  
Pleural Empyema ◽  
Important Differential Diagnosis ◽  
Uncommon Complication

Inflammatory pseudotumor of the liver (IPTL) is a rare condition, but an important differential diagnosis of hepatic space-occupying lesions. It may regress spontaneously and mimic other liver tumors. Complications are usually intrahepatic. Herein, we present a case of IPTL which developed pleural empyema and lung necrosis as an uncommon complication.

scholarly journals Urrets-Zavalia syndrome after deep anterior lamellar keratoplasty

2016 ◽  
Vol 73 (10) ◽  
pp. 973-975
Author(s):  
Vesna Jovanovic ◽  
Ljubisa Nikolic
Keyword(s):  
Case Report ◽  
Penetrating Keratoplasty ◽  
Secondary Glaucoma ◽  
Lamellar Keratoplasty ◽  
Deep Anterior Lamellar Keratoplasty ◽  
Pigment Layer ◽  
Anterior Lamellar Keratoplasty ◽  
Corneal Hydrops ◽  
Iris Atrophy ◽  
Uncommon Complication

Introduction. Urrets-Zavalia syndrome is an uncommon complication of the deep anterior lamellar keratoplasty in keratoconus. The manifestations of this syndrome are an irreversible mydriasis, iris atrophy and secondary glaucoma. Case report. Deep anterior lamellar keratoplasty was done for keratoconus with a presumably healed corneal hydrops in a 21-year-old Caucasian man. The graft remained clear, but the surgery was complicated by a fixed, dilated pupil, patches of iris atrophy, ectropium of the iris pigment layer and glaukomflecken in the lens. Conclusion. Although safer than penetrating keratoplasty, the deep anterior lamellar by not trying to secure an unhealed Descemet?s membrane with air. Instead, a new Descemet?s membrane transplanted within a penetrating graft is a safer choice.

scholarly journals Spontaneous umbilical cord hematoma causing still birth: a case report in Madagascar

2018 ◽  
Vol 7 (5) ◽  
pp. 2031
Author(s):  
Lyn Z. A. Rabetsimamanga ◽  
Hary F. Rabarikoto ◽  
Eddie B. Rekoronirina ◽  
Hery R. Andrianampanalinarivo
Keyword(s):  
Case Report ◽  
Umbilical Cord ◽  
Fetal Heart ◽  
Fetal Distress ◽  
Fetal Hypoxia ◽  
Female Fetus ◽  
Still Birth ◽  
Heart Monitoring ◽  
Short Time ◽  
Uncommon Complication

Spontaneous umbilical cord hematoma is uncommon complication during delivery. It is responsible for severe fetal distress or death. We report a case of a 28 year-old primigravida Malagasy woman at the 37th weeks of gestation. She was admitted in the delivery room for beat oscillating on the fetal heart monitoring at the beginning of labour. Cesarean section was indicated for acute fetal distress in monitoring at dilation 5cm of the cervix traduced by some decelerations.  But she gives birth to a still born female fetus by vaginal way short time after. A 5,5 cm hematoma was discovered on umbilical cord. This still birth may be due to anoxia during acute compression of the umbilical vessels by the hematoma. So, placental and cord examinations in cases of unexplained fetal hypoxia and stillbirth are very important.

scholarly journals Hemophagocytic syndrome and T-cell lymphoma after kidney transplantation: a case report

1997 ◽  
Vol 10 (6) ◽  
pp. 471-474 ◽  
Author(s):  
P. Peeters ◽  
J. Sennesael ◽  
D. Verbeelen ◽  
H. De Raeve ◽  
M. DeWaele
Keyword(s):  
Kidney Transplantation ◽  
Case Report ◽  
T Cell ◽  
Hemophagocytic Syndrome ◽  
Cell Lymphoma ◽  
T Cell Lymphoma
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