合計: 21 |
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PMID (PMCID) | ||
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30789396 |
MALE | |
Hereditary Spherocytosis Presenting as Diffuse Bone Marrow Activation and Splenomegaly on PSMA-Targeted 18F-DCFPyL PET/CT. | ||
Gomez E, Tran PT, Pienta KJ, Pomper MG, Gorin MA, Rowe SP. Clin Nucl Med. 2019;44(4):e313-e314. |
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PSMA-targeted F-DCFPyL PET/CT was performed, which demonstrated recurrent disease in the prostatectomy bed as well as splenomegaly and mild-diffuse bone marrow activation, consistent with the patient's history of hereditary spherocytosis. | ||
30789396 |
MALE | |
Hereditary Spherocytosis Presenting as Diffuse Bone Marrow Activation and Splenomegaly on PSMA-Targeted 18F-DCFPyL PET/CT. | ||
Gomez E, Tran PT, Pienta KJ, Pomper MG, Gorin MA, Rowe SP. Clin Nucl Med. 2019;44(4):e313-e314. |
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Hereditary Spherocytosis Presenting as Diffuse Bone Marrow Activation and Splenomegaly on PSMA-Targeted 18F-DCFPyL PET/CT. | ||
29200157 |
FEMALE | Infant |
An Infant With Unusually High Unconjugated Hyperbilirubinemia Due to Coexistence of Hereditary Spherocytosis and Gilbert Syndrome. | ||
Butorac Ahel I, Baraba Dekanic K, Palcevski G, Roganovic J. J Pediatr Hematol Oncol. 2018;40(2):e127-e128. |
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Hereditary spherocytosis is the most frequent congenital hemolytic anemia and is characterized with variable degree of anemia, jaundice, and splenomegaly. | ||
28321066 (5410476) |
MALE | Young Adult |
Gilbert Syndrome with Concomitant Hereditary Spherocytosis Presenting with Moderate Unconjugated Hyperbilirubinemia. | ||
Aiso M, Yagi M, Tanaka A, Miura K, Miura R, Arizumi T, Takamori Y, Nakahara S, Maruo Y, Takikawa H. Intern Med. 2017;56(6):661-664. |
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In addition, since the laboratory findings and imaging studies revealed lysemia as well as gallstone and splenomegaly, a diagnosis of hereditary spherocytosis was made as a comorbidity. | ||
27108201 |
MIXED_SAMPLE | Adult |
Disease-modifying influences of coexistent G6PD-deficiency, Gilbert syndrome and deletional alpha thalassemia in hereditary spherocytosis: A report of three cases. | ||
Jamwal M, Aggarwal A, Kumar V, Sharma P, Sachdeva MU, Bansal D, Malhotra P, Das R. Clin Chim Acta. 2016;458:51-4. |
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Hereditary spherocytosis (HS) is a common inherited hemolytic anemia characterized by heterogeneous clinical presentations with variable degrees of anemia, jaundice, splenomegaly and gallstones. | ||
27566068 (5002123) |
MALE | Middle Aged |
Open-heart surgery using a centrifugal pump: a case of hereditary spherocytosis. | ||
Matsuzaki Y, Tomioka H, Saso M, Azuma T, Saito S, Aomi S, Yamazaki K. J Cardiothorac Surg. 2016;11(1):138. |
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Hereditary spherocytosis is a genetic, frequently familial hemolytic blood disease characterized by varying degrees of hemolytic anemia, splenomegaly, and jaundice. | ||
27906107 (5134285) |
FEMALE | Adult |
Previously undiagnosed hereditary spherocytosis in a patient with jaundice and pyelonephritis: a case report. | ||
Tateno Y, Suzuki R, Kitamura Y. J Med Case Rep. 2016;10(1):337. |
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The classical clinical features of hereditary spherocytosis are anemia, jaundice, and splenomegaly. | ||
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. |
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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. | ||
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. |
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This is a report of an 11 years old male diagnosed case of hereditary spherocytosis who presented with jaundice, splenomegaly and cholelithiasis. | ||
20924216 (3304593) |
MALE | Adult |
A case of concomitant Gilbert's syndrome and hereditary spherocytosis. | ||
Lee HJ, Moon HS, Lee ES, Kim SH, Sung JK, Lee BS, Jeong HY, Lee HY, Eu YJ. Korean J Hepatol. 2010;16(3):321-4. |
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We describe moderate hyperbilirubinemia in a 28-year-old man who suffered from gallstones and splenomegaly, with combined disorders of hereditary spherocytosis (HS) and Gilbert's syndrome (GS). | ||
20618221 |
MALE | Child |
Orthotopic heart transplantation in a child with hereditary spherocytosis. | ||
Johnson CE, Schmitz ML, McKamie WA, Edens RE, Imamura M, Jaquiss RD. Artif Organs. 2010;34(12):1154-6. |
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Hereditary spherocytosis (HS) is a genetic, frequently familial hemolytic blood disease that presents with varying degrees of hemolytic anemia, splenomegaly, and jaundice.The disease arises as a result of defects in any of a number of proteins responsible for maintaining the shape and flexibility of the red blood cell, resulting in an osmotically fragile and characteristically spherical red blood cell. | ||
19740448 (2753340) |
MALE | Infant |
Complications of Evans' syndrome in an infant with hereditary spherocytosis: a case report. | ||
Yoshida H, Ishida H, Yoshihara T, Oyamada T, Kuwana M, Imamura T, Morimoto A. J Hematol Oncol. 2009;2:40. |
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Hereditary spherocytosis (HS) is a genetic disorder of the red blood cell membrane clinically characterized by anemia, jaundice and splenomegaly. | ||
18397616 |
MIXED_SAMPLE | |
[Laparoscopic splenectomy in children with hereditary spherocytosis]. | ||
Petersen CR, Bulut O, Jess P. Ugeskr Laeger. 2008;170(11):925-6. |
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Based on the positive international experience with laparoscopic splenectomy on a large number of patients since 1991, we treated two teenagers with symptomatic hereditary spherocytosis and moderate splenomegaly. | ||
12403390 |
MALE | Middle Aged |
Extramedullary paraspinal hematopoiesis in hereditary spherocytosis. | ||
De Backer AI, Zachee P, Vanschoubroeck IJ, Mortele KJ, Ros PR, Kockx MM. JBR-BTR. 2002;85(4):206-8. |
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We report on a 60-year-old man with hereditary spherocytosis who presented with an extramedullary paraspinal hematopoietic mass, splenomegaly, and bone marrow expansion in the right distal femur and proximal tibia metaphysis. | ||
12590727 |
FEMALE | Adult |
Urgent laparoscopic splenectomy in a morbidly obese pregnant woman: case report and literature review. | ||
Allran CF Jr, Weiss CA 3rd, Park AE. J Laparoendosc Adv Surg Tech A. 2002;12(6):445-7. |
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Here, we present a case of successful LS in a morbidly obese pregnant woman with splenomegaly and hemolysis secondary to hereditary spherocytosis. | ||
9168768 |
FEMALE | |
Concomitant laparoscopic cholecystectomy and splenectomy for surgical management of hereditary spherocytosis. | ||
Patton ML, Moss BE, Haith LR Jr, Shotwell BA, Milliner DH, Simeone MR, Kraut JD, Patton JN. Am Surg. 1997;63(6):536-9. |
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In conclusion, we present a combined laparoscopic cholecystectomy and splenectomy for hereditary spherocytosis associated with splenomegaly, cholelithiasis, and cholecystitis. | ||
9426643 |
MALE | Middle Aged |
Does a patient with hereditary spherocytosis qualify for preoperative autologous blood donation? | ||
Weinstein R, Martinez R, Hassoun H, Palek J. Transfusion. 1997;37(11-12):1179-83. |
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Hereditary spherocytosis (HS) is characterized by osmotically fragile spherocytic red cells (RBCs), mild to moderate hemolysis, and splenomegaly. | ||
9595784 |
MIXED_SAMPLE | Adult |
[Video laparoscopic splenectomy in a patient with splenomegaly due to hereditary spherocytosis: report of two cases]. | ||
Machado MA, da Rocha JR, Bove C, Herman P, Machado MC. Rev Hosp Clin Fac Med Sao Paulo. 1997;52(5):276-8. |
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[Video laparoscopic splenectomy in a patient with splenomegaly due to hereditary spherocytosis: report of two cases]. | ||
8840460 |
MALE | Adult |
Laparoscopic splenectomy aided by balloon occlusion of the splenic artery: report of a case. | ||
Yamashita H, Ohuchida J, Shimura H, Aibe H, Honda H, Kuroki S, Chijiiwa K, Tanaka M. Surg Laparosc Endosc. 1996;6(4):326-9. |
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For safe and efficient laparoscopic splenectomy, we performed balloon occlusion of the splenic artery with the interventional angiographic technique in a patient with hereditary spherocytosis and splenomegaly. | ||
8471774 |
FEMALE | Adult |
Human erythrocyte protein 4.2 deficiency associated with hemolytic anemia and a homozygous 40glutamic acid-->lysine substitution in the cytoplasmic domain of band 3 (band 3Montefiore). | ||
Rybicki AC, Qiu JJ, Musto S, Rosen NL, Nagel RL, Schwartz RS. Blood. 1993;81(8):2155-65. |
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Red blood cell (RBC) protein 4.2 deficiency is often associated with a moderate nonimmune hemolytic anemia, splenomegaly, and osmotically fragile RBCs resembling, but not identical to, hereditary spherocytosis (HS). |