|
Total: 5 |
|
| PMID (PMCID) | ||
|---|---|---|
|
29415937 |
MALE | Adult |
| [Portal vein thrombosis associated with idiopathic hypereosinophilic syndrome]. | ||
|
Kaito S, Harada S, Tsukada M, Kojima A, Iwama K, Yamada K, Kajiwara K, Morikawa K, Shimizu K, Kozai Y, Koudo H. Rinsho Ketsueki. 2018;59(1):45-50. |
||
| A 35-year-old man who previously underwent splenectomy for hereditary spherocytosis at age 29 visited our hospital complaining of fatigue that had started 7 days ago and right upper abdominal pain. | ||
|
29096349 (5686225) |
OTHER | |
| Extramedullary Hematopoiesis Mimicking Mediastinal Tumor in a Patient with Hereditary Spherocytosis: Case report. | ||
|
Park JB, Lee SA, Kim YH, Lee WS, Hwang JJ. Int J Surg Case Rep. 2017;41:223-225. |
||
| A 45-year-old man who presented with anemia, jaundice and abdominal pain was diagnosed with hereditary spherocytosis. | ||
|
27423290 |
MALE | Child |
| Hereditary Spherocytosis with Splenomegaly and Cholelithiasis in a Young Male of Western Region of Nepal - A Case Report. | ||
|
Ghimire P, Gurung NV, Shrestha S, Poudel SR, Chapagain A. Kathmandu Univ Med J (KUMJ). 2015;13(52):366-8. |
||
| Hereditary spherocytosis is an autosomal dominant congenital hemolytic anemia due to defect in RBC membrane protein that commonly presents with intermittent jaundice, anemia, abdominal pain, splenomegaly and sometimes cholelithiasis. | ||
|
23632607 |
MALE | Adult |
| A cholestatic diagnostic dilemma. | ||
|
Kalinke L, Rashid M. BMJ Case Rep. 2013;2013:. |
||
| A 28-year-old man with hereditary spherocytosis presented with abdominal pain and jaundice. | ||
|
24051978 |
FEMALE | Child |
| Conservative management of accessory spleen torsion in children. | ||
|
Scire G, Zampieri N, El-Dalati G, Camoglio FS. Minerva Pediatr. 2013;65(4):453-6. |
||
| In April 2009 we observed a 10-year-old child affected by hereditary spherocytosis who reported acute abdominal pain without fever or vomiting. | ||