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INTRODUCTION Thrombotic thrombocytopenic purpura (TTP) is a rare disorder with an incidence of 4–5 cases per million per year. It has significant morbidity and mortality if left untreated. Timely diagnosis and availability of effective treatment such as plasma exchange therapy have reduced the morbidity and mortality significantly. Usually, it is idiopathic or autoimmune, but several predisposing factors have been described to cause secondary TTP. In this case report, we discussed a very rare presentation of TTP secondary to dengue virus infection and how the timely diagnosis along with the immediate institution of appropriate management helped us to cure the patient. CASE REPORT A 35-year-old female with no other comorbidities was admitted to the hospital with complaints of fever and vomiting over 1 week. Her investigations revealed a low platelet count and dengue IgG, and IgM antibodies were positive. She was symptomatically treated at a local hospital and was transfused 16 units of random donor platelets over a period of 6 days. But despite this, platelet count was remaining low. Her consciousness deteriorated on the 6th day of hospital stay. Hence, she was shifted to our tertiary care center.

bodies were positive. She was symptomatically treated at a local hospital and was transfused 16 units of random donor platelets over a period of 6 days. But despite this, platelet count was remaining low. Her consciousness deteriorated on the 6th day of hospital stay. Hence, she was shifted to our tertiary care center. On arrival, the patient was drowsy, arousable to verbal commands only, and had decreased limb movement on the right side. Laboratory investigations were showing anemia, thrombocytopenia, and increased lactate dehydrogenase (LDH) level as shown in Table 1. Her peripheral blood smear revealed numerous schistocytes and computed tomography (CT) brain was unremarkable. Ultrasonography abdomen was suggestive of bulky kidneys, and she was retrovirus negative. Table 1 Laboratory findings With this clinical picture and laboratory findings, she was diagnosed as a case of TTP and was advised urgent plasma exchange therapy. Although there is no firm recommendation for administration of steroids in TTP, we started her on low-dose injection methylprednisolone (100 mg daily) considering its autoimmune etiology. Plasmapheresis was done daily with approximately 2–2.5 L plasma exchange. On the 2nd day of the admission, she had an episode of convulsion which was treated with anticonvulsive medication. She required intubation and ventilatory support because of postconvulsion low Glasgow Coma Scale (GCS).

g its autoimmune etiology. Plasmapheresis was done daily with approximately 2–2.5 L plasma exchange. On the 2nd day of the admission, she had an episode of convulsion which was treated with anticonvulsive medication. She required intubation and ventilatory support because of postconvulsion low Glasgow Coma Scale (GCS). Her antinuclear antibody result was negative. She convulsed again on 3rd day with drop in hemoglobin and platelets [Table 1], so injection rituximab 500 mg was added to treatment in addition to plasma exchange. Her CT scan of the brain was repeated which revealed no significant abnormality. Daily plasma exchange was continued. Her general condition started improving from 4th day of hospital stay. Platelet count improved, serum LDH level showed decline over a period [Table 1]. She was extubated on the 8th day. She underwent total eight plasmapheresis cycles, and before discharge, her platelet counts were 152 mm3, serum LDH was 511 U/L. She was conscious with GCS of 15/15 and without any sensory-motor deficit. We followed her up in the outpatient department, and at 6 months, she is well with normal hemogram. RESULT This patient had dengue viral infection confirmed by serology which was complicated by TTP during the acute phase of dengue viral infection. We diagnosed this by clinical features and ruling out other differential diagnosis by laboratorial and radiological tests. The patient responded well to the plasma exchange therapy with complete recovery from symptoms and no recurrence after 6 months follow-up.

d by TTP during the acute phase of dengue viral infection. We diagnosed this by clinical features and ruling out other differential diagnosis by laboratorial and radiological tests. The patient responded well to the plasma exchange therapy with complete recovery from symptoms and no recurrence after 6 months follow-up. DISCUSSION Dengue is most rapidly spreading mosquito-borne viral disease in the world. There is a global pandemic with worldwide distribution.[1] This infection has potential to cause significant morbidity and mortality.[2] Usually, it presents as mild/asymptomatic type of infection; however, at times, it may manifest in more severe forms such as dengue hemorrhagic fever, or dengue shock syndrome.[3] Many unusual complications have been observed with dengue viral infection such as hepatic damage, cardiomyopathy, and encephalopathy.[4] The presence of TTP with dengue viral infection is very rare presentation and has been reported in very few case reports.[56]

as dengue hemorrhagic fever, or dengue shock syndrome.[3] Many unusual complications have been observed with dengue viral infection such as hepatic damage, cardiomyopathy, and encephalopathy.[4] The presence of TTP with dengue viral infection is very rare presentation and has been reported in very few case reports.[56] TTP itself is a rare clinical syndrome characterized by fever, microangiopathic hemolytic anemia, thrombocytopenia, central nervous system involvement, and renal impairment. However, all five features are observed in only 40% of patients.[7] Secondary TTP can occur after infections, medications (e.g., clopidogrel, cyclosporine), autoimmune diseases, malignancies, pregnancy, and bone marrow transplantation.[8] Infections known to cause thrombotic microangiopathy include hepatitis C, parvovirus B19 virus infection, HIV infection as well as patient with dental foci or streptococci infection.[910111213] Pathophysiology of TTP includes deficiency of protease enzyme (ADAMTS13) that cleaves von Willebrand factor (vWF) in small segments. In the absence of ADAMTS13 enzyme, large vWF cause platelet aggregation and fibrin deposition in small vessels and result in microthrombi.

ental foci or streptococci infection.[910111213] Pathophysiology of TTP includes deficiency of protease enzyme (ADAMTS13) that cleaves von Willebrand factor (vWF) in small segments. In the absence of ADAMTS13 enzyme, large vWF cause platelet aggregation and fibrin deposition in small vessels and result in microthrombi. In our case, the patient was diagnosed as having dengue viral infection by the presence of IgM and IgG antibodies and treated accordingly with fluid resuscitation and platelet transfusion. But later, the patient showed features such as fever, thrombocytopenia, hemolytic anemia, and neurological involvement in the form of decreased consciousness, hemiparesis, and seizures (CT brain-normal). All these features were suggestive of TTP and patient responded well to plasma exchange therapy, steroid therapy, and injection rituximab. CONCLUSION Although the exact incidence of TTP in dengue viral infection is not known, such cases are reported in the recent past. Hence, special attention must be given to dengue virus infection patients presenting with signs and symptoms of TTP in the future. The prompt clinical recognition of such complication and early initiation of specific therapy with plasma exchange is likely to improve the patient's outcome. Financial support and sponsorship Nil. Conflicts of interest There are no conflicts of interest.