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Passenger lymphocyte syndrome in a bidirectional ABO-mismatched renal transplant
被引:6
|作者:
Prethika, P. A.
[1
]
Shastry, Shamee
[1
]
Mohan, Ganesh
[1
]
Prabhu, Ravindra Attur
[2
]
Nagaraju, Shankar Prasad
[2
]
Rangaswamy, Dharshan
[2
]
机构:
[1] Manipal Acad Higher Educ, Kasturba Med Coll, Dept Immunohematol & Blood Transfus, Manipal 576104, Karnataka, India
[2] Manipal Acad Higher Educ, Kasturba Med Coll, Dept Nephrol, Manipal, Karnataka, India
关键词:
ABO antibodies;
B lymphocyte;
direct Coombs test;
hemolysis;
passenger lymphocyte syndrome;
renal transplantation;
LIVER;
D O I:
10.4103/ajts.AJTS_98_19
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Passenger lymphocyte syndrome (PLS), a subtype of graft-versus-host disease, is due to the production of antibodies by the donor "passenger" B lymphocytes against recipient's red cells. It is a rare disorder encountered mostly in ABO blood group-mismatched solid organ transplantation. The present case report illustrates the clinical presentation and the mode of management of PLS in a bidirectional ABO-incompatible renal transplantation. A 43-year-old male diagnosed with chronic kidney disease Stage 5-D (diabetic nephropathy) Type-2 hypertension with ischemic heart disease underwent ABO bidirectional-mismatched renal transplantation. The blood group of the patient was B Rh D positive and that of the donor (patient's wife) was A Rh D positive. In the pretransplantation phase, immunoglobulin G anti-A titer was 64 by column agglutination method, which was subsequently brought down to 4 by therapeutic plasma exchange and immunosuppression. Good graft function was established in the posttransplantation phase, but a significant drop in the hemoglobin (Hb) was noted. A fall in Hb, peripheral smear findings suggestive of hemolysis, and direct antiglobulin test positivity along with raised lactate dehydrogenase suggested the diagnosis of PLS; the patient was managed successfully for the same by transfusion of O blood group packed red blood cell transfusion and immunosuppression. PLS is a rare but important cause of immune-mediated hemolytic anemia in ABO-mismatched transplants.
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页码:63 / 66
页数:4
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