□ CASE REPORT □ Malignant Hypertension with Thrombotic Microangiopathy Hayato Mitaka 1, Yuji Yamada 2, Osamu Hamada 3, Shintaro Kosaka 3, Naoki Fujiwara 3 and Yoshitaka Miyakawa 3,4 Abstract A 49-year-old man with malignant hypertension, acute kidney injury and mental deterioration was referred to our hospital. We initially observed microangiopathic hemolytic anemia, thrombocytopenia and kidney dam- age, indicating he had thrombotic microangiopathy (TMA). We considered TMA was caused by malignant hypertension and therefore did not start plasma therapy. The French TMA reference center reported that plate- let counts and serum creatine levels have high values for predicting severe ADAMTS13 deficiency. The pa- tient fully recovered from his illness after treatment with antihypertensive drugs and intermittent hemodialy- sis. This case might thus be useful to understand the proper differential diagnosis and treatment of TMA. Key words: thrombotic microangiopathy, malignant hypertension, hypertensive emergency (Intern Med 55: 2277-2280, 2016) (DOI: 10.2169/internalmedicine.55.6332) If patients who present with an altered mental status and Introduction impaired renal function develop TMA, then empirical ther- apy with plasma exchange or plasma infusion should be ini- Thrombotic microangiopathy (TMA) describes a patho- tiated in most cases due to the difficulty in ruling out TTP logical process of microvascular thrombosis, consumptive at presentation. Although this approach has been widely ac- thrombocytopenia, and microangiopathic hemolytic anemia cepted (2, 3), unnecessary and potentially harmful plasma (MAHA), leading to ischemic organ damage (1). TMA syn- exchange or plasma infusion should be avoided if possible. drome is divided into primary TMA and secondary We herein present a case of TMA caused by malignant hy- TMA (1). The syndromes of primary TMA have defined ab- pertension. We experienced a favorable clinical outcome in normalities that require specific treatment, such as our patient without plasma exchange according to careful ADAMTS13-mediated TMA [also known as thrombotic consideration of the differential diagnosis from TTP by pre- thrombocytopenic purpura (TTP)], Shiga toxin-mediated dicting the ADAMTS13 activity from high platelet counts TMA [also known as hemolytic uremic syndrome (HUS)], and elevated serum creatine levels based on the previous drug-mediated TMA, complement-mediated TMA (atypical study by the French TMA reference center (4). HUS), and cobalamin-mediated TMA (1). Secondary TMA syndrome is caused by some underlying disease, such as in- Case Report fection and collagen disease. These diseases include malig- nant hypertension, preeclampsia, hemolysis, elevated liver A 49-year-old man with a history of untreated hyperten- enzyme, and low platelets (HELLP) syndrome, systemic in- sion was admitted to another hospital with shortness of fections, malignancies, autoimmune disorders (such as sys- breath, an extremely high blood pressure of 240/140 mmHg, temic lupus erythematosus, antiphospholipid antibody syn- and evidence of acute kidney injury (blood urea nitrogen, drome, and scleroderma renal crisis), hematopoietic stem 141 mg/dL; serum creatinine, 8.95 mg/dL; positive granular cell or organ transplantation, and disseminated intravascular cast). He was originally diagnosed as having hypertension coagulopathy (1). when he was approximately 30 years of age. His blood pres- １Department of Internal Medicine, Tokyo Bay Urayasu Ichikawa Medical Center, Japan, ２Department of Medicine, Mount Sinai Beth Israel, USA, ３Department of General Internal Medicine, Nerima Hikarigaoka Hospital, Japan and ４Department of General Internal Medicine, Saitama Medical University, Japan Received for publication August 8, 2015; Accepted for publication December 15, 2015 Correspondence to Dr. Yoshitaka Miyakawa, [email protected] 2277 Intern Med 55: 2277-2280, 2016 DOI: 10.2169/internalmedicine.55.6332 Figure 1. Funduscopic examination. Papilledema, retinal Figure 2. Magnetic resonance imaging of the head. High in- hemorrhage, soft exudate, and copper wire arterioles can be tensity signals in the bilateral cerebral white matter on fluid- seen, suggesting hypertensive retinopathy. attenuated inversion recovery is observed, suggesting posterior reversible encephalopathy syndrome (PRES). sure had been well controlled until he self-discontinued a calcium channel blocker 5 years previously. He had no ane- gesting leukoencephalopathy (data not shown). Magnetic mia, thrombocytopenia or kidney damage on a previous an- resonance imaging of the brain showed high intensity sig- nual routine health examination. nals in the bilateral cerebral white matter on T2-weighted After he was admitted to the previous hospital, he was di- images and fluid-attenuated inversion recovery with an in- agnosed with malignant hypertension and treated with intra- crease in the apparent diffusion coefficient, compatible with venous furosemide, oral amlodipine, and candesartan. De- posterior reversible encephalopathy syndrome (PRES) spite this treatment, he had a worsening renal function and (Fig. 2). Abdominal computed tomography showed normal- gradually developed an altered mental status. Four days sized kidneys without hydronephrosis. later, he was referred to our hospital for urgent hemodialy- According to these findings, the patient was diagnosed sis. He did not have a recent history of infectious gastroen- with malignant hypertension. Emergent dialysis was per- teritis or diarrhea. On this physical examination, his blood formed and intravenous antihypertensive therapy with pressure was 170/84 mmHg, pulse was 86 beats per minute, nicardipine was initiated to achieve a normal blood pressure respiratory rate was 16 breaths per minute, oxygen satura- within several days. We presumed that ADAMTS13- tion was 98% while he was breathing ambient air, and body deficinent TTP was unlikely, as his platelet counts (97×109/ temperature was 36.0℃. His Glasgow Coma Scale was 13 L) and serum creatinine levels (11.0 mg/dL) at presentation (E3V4M6) without notable focal neurological signs. A fun- were elevated according to the cut-off values provided in the duscopic examination showed hypertensive retinopathy, indi- previous report by the French TMA reference center (4). cating he had hypertension for a certain time (Fig. 1). The With several courses of intermittent hemodialysis and rest of the examinations were unremarkable. control of his blood pressure, the patient’s altered mental A complete blood count showed that the white blood cell status completely resolved, and thrombocytopenia and the count was 7,700/μL with 84% neutrophils and 5% lympho- renal function dramatically improved (Fig. 3). It took 7 days cytes, hemoglobin level was 10.4 mg/dL, and the platelet until we obtained the results of the ADAMTS13 activity and count was 97×109/L. A peripheral blood smear revealed inhibitor, because it was not covered by the Japanese public more than two schistocytes per high-power field without health insurance. The ADAMTS13 activity was 61% and leukemic blast cells. The blood urea nitrogen level was ADAMTS13 inhibitors were negative, indicating that TTP 148.1 mg/dL and the creatinine level was 11.0 mg/dL. The was excluded. A stool culture was negative for Shiga toxin- lactate dehydrogenase (LDH) level was 473 IU/L. Liver producing Escherichia coli. The serum cobalamin levels function tests were normal. The prothrombin time, activated were within the normal limits. Antinuclear antibody, an- partial thromboplastin time, and serum fibrinogen and FDP tiphospholipid antibody, and antineutrophil cytoplasmic anti- levels were within normal limits. The D-dimer level was body were negative. These findings excluded HUS, cobala- only slightly increased to 1.1 μg/mL. The serum haptoglobin min deficiencies, and collagen diseases. Although his serum level was low and a direct Coombs test was negative, indi- creatinine level remained as high as 4-5 mg/dL, we success- cating non-immunological hemolytic anemia. Disseminated fully stopped intermittent hemodialysis. On hospital day 40, intravascular coagulation (DIC) was excluded according to he was discharged from the hospital with normal platelet the results from these laboratory tests. counts. A standard work-up for secondary hypertension, Computed tomography of the head revealed bilateral such as renovascular hypertension, primary aldosteronism, broad low-density areas in the cerebral white matter, sug- Cushing syndrome, pheochromocytoma, hypothyroidism, 2278 Intern Med 55: 2277-2280, 2016 DOI: 10.2169/internalmedicine.55.6332 Figure 3. In-hospital clinical course. Thrombocytopenia and the renal function were dramatically improved after the initiation of antihypertensive therapy and intermittent hemodialysis. and hyperthyroidism, was performed. However, the screen- dard deviation), 17.4 (14.2)×109/μL] compared with those ing tests were all negative other than subclinical hyperthy- in the ADAMTS13 detectable group [66.6 (49.3)×109/μL]. roidism, which returned to a euthyroid status during the Additionally, the serum creatinine levels were significantly follow-up. Therefore, we concluded that the patient’s malig- lower in the deficiency group [1.29 (0.77) mg/dL] than in nant hypertension was derived from untreated essential hy- the detectable group [5.13 (3.68) mg/dL] (4). pertension. Recently, Kato et al. developed a new immunoassay to rapidly measure the ADAMTS13 activity using gold parti- Discussion cles and an automated machine (7).