scholarly journals Hemophagocytic lymphohistiocytosis and visceral leishmaniasis in children: case report and systematic review of literature

2016 ◽  
Vol 10 (01) ◽  
pp. 103-108 ◽  
Author(s):  
Maria Scalzone ◽  
Antonio Ruggiero ◽  
Stefano Mastrangelo ◽  
Giovanna Trombatore ◽  
Vita Ridola ◽  
...  

Hemophagocytic lymphohistiocytosis is a potentially fatal disorder resulting from excessive activation and non-malignant proliferation of T lymphocytes and macrophages. Neoplasms, autoimmune disorders and systemic infections can cause secondary hemophagocytic syndrome. The association of hemophagocytic syndrome and visceral leishmaniasis is rarely found in childhood.  We report a case of an infant affected by hemophagocytic lymphohistiocytosis secondary to visceral leishamniasis and describe all cases of hemophagocytic syndrome associated with visceral leishamniasis in childhood reported in literature, focusing on clinical manifestation, diagnosis and treatment.

2008 ◽  
Vol 56 (5) ◽  
pp. 381-388 ◽  
Author(s):  
Srinivas Rajagopala ◽  
Usha Dutta ◽  
K.S. Poorna Chandra ◽  
Prateek Bhatia ◽  
Neelam Varma ◽  
...  

2016 ◽  
Vol 14 (4) ◽  
pp. e435-e439 ◽  
Author(s):  
Wei Keith Tan ◽  
Mae-Yen Tan ◽  
Wei Shen Tan ◽  
Soon Ching Gan ◽  
Rajadurai Pathmanathan ◽  
...  

2021 ◽  
Vol 14 (12) ◽  
pp. e246005
Author(s):  
Louise Gurowich ◽  
Gabriel Yiin ◽  
Adam Maxwell ◽  
Alexandra Rice

Myasthenia gravis (MG) is an autoimmune condition affecting the neuromuscular junction characterised by weakness and fatiguability, carrying a high morbidity if treatment is delayed. A clear association with thymoma has led to management with thymectomy as a common practice, but MG presenting post-thymectomy has rarely been reported. We present a case of an 82- year-old woman developing fatigue, ptosis and dysarthria 3 months after thymectomy. After a clinical diagnosis of MG was made, she responded well to prompt treatment with prednisolone and pyridostigmine. Her anti-acetylcholine receptor antibody (anti-AChR) subsequently came back positive. Our systematic review reveals that post-thymectomy MG can be categorised as early-onset or late-onset form with differing aetiology, and demonstrated correlation between preoperative anti-AChR titres and post-thymectomy MG. The postulated mechanisms for post-thymectomy MG centre around long-lasting peripheral autoantibodies. Clinicians should actively look for MG symptoms in thymoma patients and measure anti-AChR preoperatively to aid prognostication.


Infection ◽  
2019 ◽  
Vol 47 (4) ◽  
pp. 507-518 ◽  
Author(s):  
Francesca Rinaldi ◽  
Susanna Giachè ◽  
Michele Spinicci ◽  
Paola Corsi ◽  
Silvia Ambu ◽  
...  

2020 ◽  
Vol 5 (2) ◽  
pp. 49-58 ◽  
Author(s):  
Bárbara Brambilla ◽  
Amanda Machado Barbosa ◽  
Cassiano da Silva Scholze ◽  
Floriano Riva ◽  
Lislene Freitas ◽  
...  

2020 ◽  
Vol 23 (4) ◽  
pp. 589-594 ◽  
Author(s):  
Saket Jha ◽  
Amal Basnet ◽  
Rajiv Ranjan Kumar ◽  
Aadhaar Dhooria ◽  
Venkata Subramanian Krishnaraju ◽  
...  

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