aplastic anaemia
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2021 ◽  
Vol 2021 ◽  
pp. 1-7
Author(s):  
Synne Dragesund Rørvik ◽  
Kristoffer Stange Larsen ◽  
Lars Helgeland ◽  
Håvard Dale ◽  
Birgitta Ivarsen ◽  
...  

Introduction. Necrotizing soft tissue infections are rapidly progressing infections associated with severe inflammation and cytokine release. Early recognition and surgical intervention are key factors to secure survival. The current case presents a patient with multifocal necrotizing soft tissue infection as the initial presentation of severe aplastic anaemia. Case Presentation. A man in his fifties was admitted with septic shock with multiorgan failure and severe pancytopenia, after two days of malaise with high fever and right flank pain. The diagnosis streptococcal necrotizing myositis was significantly delayed due to atypical clinical findings. After initial surgical exploration, the decision was made to defer from surgical debridement due to extensive involvement of several muscle groups, grave pancytopenia, and suspected dismal prognosis. Surprisingly, the patient stabilized after antibiotics and intensive care treatment. Based on severe pancytopenia and hypocellular bone marrow, with no evidence of other bone marrow disorders, the patient was diagnosed with aplastic anaemia. Treatment for aplastic anaemia with antithymocyte globulin, cyclosporine, and eltrombopaq was started, and 2 months later, a partial haematological recovery was observed. The patient could be discharged from hospital without antibiotic treatment. Conclusions. This case illustrates the crucial role of a multidisciplinary approach on admission and further during the clinical course. Clinical improvement despite severe neutropenia and stabilization during immunosuppressive therapy suggest that immunological factors modulate clinical course in necrotizing soft tissue infections.


Author(s):  
Nicola Cecchi ◽  
Juri Alessandro Giannotta ◽  
Wilma Barcellini ◽  
Bruno Fattizzo

Haematologica ◽  
2021 ◽  
Author(s):  
Daniele Avenoso ◽  
Judith C W Marsh ◽  
Victoria Potter ◽  
Antonio Pagliuca ◽  
Simon Slade ◽  
...  
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Author(s):  
Aruna Barade ◽  
Fouzia Aboobacker ◽  
Anu Korula ◽  
Kavitha Lakshmi ◽  
Anup Devasia ◽  
...  

Author(s):  
Noriharu Nakagawa ◽  
Ken Ishiyama ◽  
Mikoto Tanabe ◽  
Takeshi Yoroidaka ◽  
Hiroki Mizumaki ◽  
...  

Author(s):  
Khaled Saleh Ben Salah ◽  
Khaled Saleh Ben Salah ◽  
Abdulfattah A Elturki ◽  
Yuossef Swaisi ◽  
Fatma M. Emaetig ◽  
...  

Aplastic anaemia is a severe haematological disorder characterized by an inadequate number of hematopoietic stem cells, resulting in pancytopenia, formed by a hypocellular bone marrow. Disorders of this nature are widely treated with haematopoietic stem cell transplantation (HSCT). A potential chronic complication following (HSCT) is the growth of secondary malignancies. Notably, patients suffering from chronic graft versus host disease (cGvHD) secondary to HSCT have been shown to be more susceptible to oral squamous cell carcinoma (OSCC). Here, we present a rare case of a 30-year-old Libyan woman treated with HSCT for aplastic anaemia, with subsequent complications of cGvHD and OSCC after few months of HSCT. These carcinomatous lesions were detected in the buccal gingiva and retromolar pad area at the age of 31. The present case report emphasizes the connection between oral cGvHD and OSCC, and the potential appearance of OSCC after HSCT at any time of patient life. Thus, closer follow-up is mandatory for all patients treated with HSCT who developed cGvHD, and efficient cGvHD prevention and therapeutic approaches are needed.


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