| CASE REPORT WITH REVIEW OF LITERATURE |
|
| Year : 2020 | Volume
: 41
| Issue : 6 | Page : 909-912 |
|
|
Case report on autoimmune hemolytic anemia: A mask of malignancy!
Abhilasha Sampagar1, Neha Giridhar Patil1, Sandip Bartakke2, S Shrividya2
1 Department of Pediatrics, KAHER'S Jawaharlal Nehru Medical College, Belagavi, Karnataka, India
2 Department of Hematology, Aditya Birla Memorial Hospital, Pune, Maharashtra, India
Correspondence Address:
Dr. Abhilasha Sampagar
Pediatric Hematologist- Oncologist, Associate Professor, Department of Pediatrics, KAHER's Jawaharlal Nehru Medical College, Belagavi, Karnataka
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/ijmpo.ijmpo_182_20
|
|
|
A 10-year-old boy with autoimmune hemolytic anemia (AIHA) was treated at a local setup with repeated blood transfusions and steroids considering an idiopathic etiology. After 7 months of unresponsiveness, the child started developing recurrent fever with night sweats and pain in the abdomen which was diagnosed as tuberculosis on account of granulomatous necrotizing lesion on computed tomography (CT)-guided lymph node biopsy and treated for the same. Four months later, when the child presented to our center in anemic heart failure, work-up with positron emission tomography-CT and excisional biopsy of mesenteric lymph node led to the diagnosis of advanced Hodgkin's lymphoma with B symptoms. AIHA in pediatric age group, unlike in adults, is usually secondary. Our report stresses on a thorough evaluation of AIHA as it can mask a malignancy for a long duration and alter its course if treated with steroids, making the patient resistant to further chemotherapy.
|
|
|
|
| [FULL TEXT] [PDF]* |
|
 |
|
