scholarly journals A rare case of hereditary angioedema: C1 esterase deficiency syndrome

2016 ◽  
Vol 0 (0) ◽  
pp. 0
Author(s):  
Anuj Singhal ◽  
DarshanSingh Bhakuni ◽  
Rahul Tyagi ◽  
AjayKumar Sharma
Keyword(s):  
Hereditary Angioedema ◽  
Rare Case ◽  
Deficiency Syndrome

scholarly journals A rare case of hereditary angioedema: C1 esterase deficiency syndrome

2016 ◽  
Vol 11 (4) ◽  
pp. 236
Author(s):  
Anuj Singhal ◽  
DarshanSingh Bhakuni ◽  
Rahul Tyagi ◽  
AjayKumar Sharma
Keyword(s):  
Hereditary Angioedema ◽  
Rare Case ◽  
Deficiency Syndrome

scholarly journals Gastrointestinal histoplasmosis mimicking peritonitis carcinomatosis: a rare case of an emergent surgical presentation of HIV de novo

2019 ◽  
Vol 2019 (10) ◽  
Author(s):  
Esmee W M Engelmann ◽  
Jelle J Posthuma ◽  
Lianne Scholten ◽  
Louise L Blankensteijn ◽  
Mireille B Boldewijn ◽  
...  
Keyword(s):  
Rare Case ◽  
De Novo ◽  
Immune Deficiency Syndrome ◽  
Acquired Immune Deficiency Syndrome ◽  
Deficiency Syndrome ◽  
Healthy Patient ◽  
Disseminated Histoplasmosis ◽  
Gastrointestinal Histoplasmosis ◽  
Acquired Immune Deficiency ◽  
Apparently Healthy

Abstract Gastrointestinal perforation due to infection, including disseminated histoplasmosis, is a rare cause of the surgical acute abdomen, especially in an apparently healthy patient. We describe a rare case of gastrointestinal histoplasmosis-induced small intestine perforation as the first manifestation of acquired immune deficiency syndrome in a healthy patient. Remarkably, the disease mimicked peritonitis carcinomatosis during explorative laparoscopy.

Rare Case of Hereditary Angioedema in a Male With Normal C1 Esterase Inhibitor Levels

CHEST Journal ◽  
2015 ◽  
Vol 148 (4) ◽  
pp. 648A
Author(s):  
Deepak Sharma ◽  
Varun Jain ◽  
Jessica Stoeckel
Keyword(s):  
Hereditary Angioedema ◽  
Rare Case ◽  
C1 Esterase Inhibitor ◽  
Esterase Inhibitor

scholarly journals A rare case of intussusception leading to the diagnosis of acquired immune deficiency syndrome: a case report

2009 ◽  
Vol 3 (1) ◽  
Author(s):  
Ioannis Kehagias ◽  
Stavros N Karamanakos ◽  
Spyros Panagiotopoulos ◽  
Sofia Giali ◽  
Charalambos A Gogos ◽  
...  
Keyword(s):  
Immune Deficiency ◽  
Case Report ◽  
Rare Case ◽  
Immune Deficiency Syndrome ◽  
Acquired Immune Deficiency Syndrome ◽  
Deficiency Syndrome ◽  
Acquired Immune Deficiency

scholarly journals A rare case of limb deficiency syndrome: Gollop WolfGang syndrome

2021 ◽  
Vol 16 (8) ◽  
pp. 2053-2055
Author(s):  
Ronak Hapani ◽  
Mona Shastri
Keyword(s):  
Rare Case ◽  
Deficiency Syndrome ◽  
Limb Deficiency

Identification of Pulmonary Deposits from a Sandpaper Worker: A Study by Electron Microscopy and X-Ray Microanalysis

1982 ◽  
Vol 40 ◽  
pp. 52-53
Author(s):  
S. K. Peng ◽  
M.A. Egy ◽  
J. K. Singh ◽  
M.B. Bishop
Keyword(s):  
Electron Microscopy ◽  
Environmental Pollution ◽  
Rare Case ◽  
Interstitial Fibrosis ◽  
X Ray ◽  
Documented Case ◽  
Etiologic Agents ◽  
Pulmonary Interstitial Fibrosis ◽  
Gold Miners ◽  
Pulmonary Changes

Electron microscopy and energy dispersive x-ray microanalysis (EDXA) are found to be very useful tools for identification of etiologic agents in pneumoconiosis or interstitial pulmonary disorders. Pulmonary interstitial fibrosis and granulomatosis are frequently associated with occupational and environmental pollution. Numerous reports of pneumoconiosis in various occupations such as coal and gold miners are presented in the literature. However, there is no known documented case of pulmonary changes in workers in the sandpaper industry. This study reports a rare case of pulmonary granulomatosis containing deposits from abrasives of sandpaper diagnosed by using EDXA.

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