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. 2022 Apr 9;22:136. doi: 10.1186/s12893-022-01580-5

Table 1.

Summary of hereditary spherocytosis patients with splenic infarction: a literature review

Year of publication Country Age/sex Underlying disease Fever Abdominal pain Spleno- megaly Splenic rupture Splenectomy Urgent/ selective
2007 [17] Japan 10–20/M IM YES LUA pain YES NO YES SEL
2015 [16] United Kingdom 10–20/M IM YES Left chest pain YES NO NO
2020 [9] USA 10–20/F IM YES LUA pain YES NO NO
2011 [10] United Kingdom 10–20/M SCT NO LUA pain YES NO NO
2007 [8] USA 10–20/F SCT NO LUA pain YES NO YES URG
2003 [7] USA 40–50/M SCT NO LUA pain YES NO NO
1997 [12] France 10–20/M SCT YES Left chest pain N/A NO NO
1992 [14] USA 0–10/M SCT NO LUA pain YES NO YES SEL
1992 [14] USA 10–20/M SCT NO LUA pain YES NO YES SEL
1990 [13] USA 10–20/M SCT YES LUA pain YES NO YES SEL
2008 [15] Germany 10–20/M IM and PCD YES LUA pain YES NO NO
2016 [6] China 20–30/M INS YES Left chest pain YES NO YES URG
2017 [18] Swit 10–20/M NO NO LUA pain YES NO YES URG
The present patient China 10–20/F IM YES LUA pain YES NO YES URG

IM Infectious mononucleosis, SCT Sickle cell traits, PCD Protein C deficiency, INS invasive nontyphoidal salmonellosis, LUA Left upper abdomen