Acquired Von Willebrand Syndrome (AVWS) Type 2A as the Presenting Feature of JAK2 Wild type Thrombocythemia in a Child: Effectiveness of Platelet Reduction by AnagrelideJan Jacques Michiels1*, Ulrich. Budde2 and Thomas Kuehn3
Received date: July 10, 2017; Accepted date: August 03, 2017; Published date: August 08, 2017
Citation: Michiels JJ, Budde U, Kuehn T (2017) Acquired Von Willebrand Syndrome (AVWS) Type 2A as the Presenting Feature of JAK2 Wild type Thrombocythemia in a Child: Effectiveness of Platelet Reduction by Anagrelide. J Hematol Thrombo Dis 5:274. doi: 10.4172/2329-8790.1000274
Copyright: © 2017 Michiels JJ, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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A 9-year-old Caucasian boy presented in 1994 with severe headache, attacks of migraine, aggressive behavior and minor bleeding symptoms. Initial abnormal laboratory data were a platelet count of 1596 × 109/L and slight splenomegaly on echogram. Low-dose aspirin 100 mg/day relieved the cerebral symptoms, but a pronounced spontaneous bleeding tendency became evident. Severe epistaxis, bruises, hematomas and gum bleedings resulted in an iron deficiency state (hemoglobin 5.7 mmol/L,hematocrit 0.30, MCV 77 fl, ferritine 6 ug/l) in November 1995. The combination of mucocutaneous bleeding, high platelet counts (1946 × 109/L), and increase of enlarged megakaryocytes in a bone marrow smear was consistent with the diagnosis of hemorrhagic thrombocythemia. Coagulation studies revealed the presence of an acquired von Willebrand syndrome type 2A featured by a prolonged Ivy bleeding time, near normal factor VIII coagulant activity (0.53 u/ml) and von Willebrand factor (VWF) antigen (0.55 u/ml), low VWF ristocetine cofactor activity (0.29), very low VWF collagen binding activity (0.16 u/ml) and absence of large VWF multimers. A severe epistaxis lasting for several hours stopped immediately after correction of the VWF parameters by substitution of 3000 units Bone marrow histopathology showed a pronounced increase of large immature megakaryocytes with hyperlobulated nuclei and maturation defects of nuclei and cytoplasm, and absence of reticuline fibrosis consistent with the diagnosis of JAK2 wild type thrombocythemia in primary megakaryocytic granulocytic myeloproliferation (PMGM). Initial treatment with hydroxyurea (500 mg daily) followed by anagrelide resulted in correction of platelet count from 2000 × 109/L to near normal (400-600 × 109/L) by), which was associated with relief of bleeding symptoms, and correction of plasma VWF values and VWF multimeric pattern to normal. The subsequent natural history was featured by spontaneous reduction of platelet count to near normal and no progression of JAK2 wild type myeloproliferative neoplasms for more than 13 years follow-up.
Hemorrhagic thrombocythemia; Myeloproliferative neoplasm; JAK2 wild type; Acquired Von Willebrand Disease; Essential thrombocythemia; Hydroxyurea; Anagrelide
Essential thrombocythemia (ET) with either thrombotic or bleeding manifestations as the presenting symptoms of a myeloproliferative disorder usually occurs at old age above 50 years, but also affects young adults [1-3] ET is rare in children. Clinical manifestations of microvascular circulation disturbances and/or mucocutaneous bleeding have been reported in about 26 cases with childhood ET until 2000 [4-7]. Philadelphia chromosome negative and bcr negative ET is one of the less rare variants of chronic myeloproliferative disorders [8-11]. According to the criteria of the Polycythemia Vera Study Group (PVSG) , ET is a diagnosis of exclusion other variants of myeloproliferative disease. The Thrombocythemia Vera Study Group (TVSG)  used bone marrow histology as a specific clue to the diagnosis of ET [1,2]. The use of the PVSG and TVSG criteria for the clinical diagnosis of ET (Table 1) include three types of ET in various myeloproliferative disorders when the bone marrow features according to the 2006→2008 European Clinical Molecular and Pathological (ECMP) criteria are applied (Table 1) . In this study we present a child who presented with aspirin-responsive microvascular circulation disturbances followed by spontaneous hemorrhages due to an acquired von Willebrand syndrome as the presenting feature of JAK2 wild type hypercellular ET in primary megakaryocytic granulocytic myeloproliferation (PMGM) .
Methods Hematological Investigations
Hematologic data were obtained using routine procedures. Blood and bone marrow smears were stained by the May-Grünwald-Giemsa method and processed for the periodic acid-Schiff (PAS) reaction. The leukocyte alkaline phosphatase (LAP) score was determined with the cytochemical technic of Hayhoe and Quaglino [14,15]. Bone marrow biopsies were done with a Jamshidi needle and embedded in glycol methylcrylate without decalcification. Sections were stained with hematoxylin-azophyloxin, PAS, gallamine-Giemsa, and Gomori’s reticulin method. Cytogenetic analysis followed standard procedure. Nucleated cells from peripheral blood and bone marrow aspirates were cultured for 24 and 48 hours, without addition of phytohemaglutinin but with methotrexate treatment of the cultures. All metaphases were banded with the use of G-, Q-, or R-bands and analysed according to the International System for Cytogenetic Nomenclature (ISCN) . Southern blot analysis was performed as previously reported . In brief, Bgb II, Hibd III, Bam HI and Eco RI-digested DNA was electrophoresed on a 0.7% agarose gel, blotted, and hybridized to the bcr probes, i.e., the 5’ Bgl II- Hind III bcr fragment and the 3’Hind IIIBgl II bcr fragment . The hemorrhagic thrombocythemia as the presenting manifestation of a myeloproliferative disorder was characterized according to the recently defined bone marrow features according to ECMP criteria for the diagnosis of essential thrombocythemia, polycythemia vera and primary megakaryocytic granulocytic myeloproliferation (PMGM) [2,11,14].
Hemostatic tests were performed using routine procedures. Bleeding times were measured according to Ivy et al. . Platelets were counted in EDTA blood samples using the Platelet Analyzer 810 (Baker Instruments, Allentown, PA). Platelet aggregation induced by collagen (Sigma Chemical St Louis) in optimal concentration, by ADP (Sigma Chemical St Louis ) 10-5 M f (final concentration) and 10-6 M f, by epinephrine (Sigma Chemicals St Louis) 10-6 M f and 10-6 M f and Factor VIII coagulant activity (FVIII:c) was assayed by means of the Automatic Coagulation Laboratory (ACL; Instrumental Laboratory, IJsselstein, The Netherlands) using FVIII-deficient plasma (Ortho Diagnostic Systems, Beerse, Belgium). Ristocetine (H. Lundbeck Co, Copenhagen, Denmark) induced platelet aggregation (RIPA) was recorded with the use of a serial aggregometer (Payton model 300B: Scarborough, Canada) in platelet-rich plasma at a standard count of 200 × 109/L.
Von Willebrand factor (vWF) assays
VWF antigen (VWF: Ag) was assayed by an enzyme-linked immunosorbent assay (ELISA), as described by Cejka . Ristocetin cofactor activity (vWF: RCo) was assayed with formalin-fixed platelet using a PAP4 Model Aggregometer (Bio-Data Corp. Hatboro, PA) according to MacFarlane et al. . The collagen binding activity of vWF (VWF: CBA) was measured according to the ELISA-based method of Brown and Bosak  with slight modifications by Dr Van Vliet of the Rotterdam Clinical Research Laboratory (RCRL). The collagen suspension was prepared by overnight hydration of one gram collagen (bovine achilles tendon, type I, C9879; Sigma Chemicals, St Louis, MO) in 400 ml 3% acetic acid at 4°C and homogenisation for 30 minutes in a blender. According to these procedure pellets, if any, formed after centrifugation at 2500 g for 15 minutes should be very small. The suspension should look silky and fibrous; if it looks granular homogenisation has to be repeated. Buttons and supernatant mixed by stirring were stored at 4°C. Microtiter plate wells (A/S Nunc, Roskilde, Denmark) were coated overnight at 4°C with 100 μl of a 0.2 mg/ml suspension of collagen in 20 mmol/L acetic acid. The wells were emptied, washed with phosphate-buffered saline (PBS)-0/05% Tween 20 (PBS-Tween). Subsequently, 100 μL of 1/40 dilutions of plasma in PBS-Tween-1% albumin were added to the wells and incubated for 2 hours at room temperature. After washing, the wells were incubated with 100 μL of a 1/200 dilution in PBS-Tween-Albumin of horseradish peroxidase-conjugated rabbit polyclonal Igs to human vWF (Dako A/S, Glostrup, Denmark) for another two hours at room temperature. After washing, 100 μL ABTS substrate solution [27.4 mg ABTS (2.2’-azinodi-[ 3-ethyl-benzthiazolsulphonate(8)] dissolved in 10 ml buffer, containing 10 mmol/L citric acid. 100 mmol/L Na2HO4 and 10 μL 30% H2O2 was added. After 15 minutes of incubation, the color development was stopped by the addition of 10 μL concentrated acetic acid and the extinction was measured at 414 nm. The in house VWF: CBA method by Dr van Vliet has not changed in the Rotterdam Clinical Research Laboratory (RCRL) before, during and after the period 1992 to 1998 of the presented study.
The multimeric composition of VWF by Budde (Hamburg Coagulation Lab) was analyzed using sodium dodecyl sulfate (SDS) agarose discontinuous gel electrophoresis according to Ruggeri et al with slight modifications [22,23]. Briefly, the samples were diluted between 1:10 and 1:20, according to their VWF:Ag content usng a buffer composed of 10 mmol/L Tris-HCL, 1 mmol/L EDTA, 2% SDS, ph 8.0, and subjected to electrophoresis overnight. The separated multimers were then transferred onto nitrocellulose by electroblotting with a 50 mmol/L phosphate buffer, ph 7.4, containing 0.04% SDS, and incubated sequentially with a rabbit anti-VWF antibody (Dakopatts, Hamburg, Germany) and a goat antiravbbit IgG conjugated to horseradish peroxidase (Bio-Rad, Munich, Germany). Detection of the VWF multimers by luminography was achieved by incubating the nitrocelluse membrane with 5 ml of a solution prepared by mixing 40 mg of luminal (Sigma, Munich, Germany and 10 mg 4-iodophenol (Aldrich, Munich, Germany) into 100 ml of Tris-buffered saline (20 mmol/L Tris-HCL, 500 mmol/L NaCL, ph 7.5). The luminescent blots were than covered by a translucent polyethylrene film and exposed to a Y-ray film (X-OMAT S, Kodak, Stuttgart, Germany) for 3 to 5 seconds.
Criteria for diagnosis and classification of essential thrombocythemia (ET)
Since 1992 we used the established inclusion, exclusion and confirmative criteria proposed by the TVSG  and PVSG  for the clinical diagnosis of ET (Table 1). We subsequently apply bone marrow features and European Clinical, Molecular and Pathobiological (ECMP) criteria for the classification of ET in various myeloproliferative disorders . The application of the ECMP classification distinguish three phenotypes of JAK2V617F mutated ET including: normal cellular ET, ET with features of early PV (prodromal PV, and ET associated with prefibrotic megakaryocytic granulocytic myeloproliferation: JAK2-MGM (Table 1).
A 9-year-old Caucasian boy presented in June 1994 with severe headache, attacks of migraine, aggressive behavior and minor bleeding symptoms. His past medical and familial history were unremarkable. On physical examination the tip of the spleen was palpable. The length diameter of the spleen on ultrasound scan was enlarged, length diameter 10 cm. A MRI-scan of the head and an EEG were nondiagnostic. Initial laboratory data in 1994 were hemoglobin 14 g/dl (8.75 mmol/l), ht 0.38, MCV 86 fl, platelets 1596 × 109/L, leukocytes 9 × 109/L, a normal white blood cell differential count and LDH 350 u/L. Renal and liver function tests and ferritine (28 ng/L) were normal. While on continuous low dose aspirin 100 mg/day the cerebral symptoms relieved and did not recur in 1994 and 1995, but a pronounced spontaneous bleeding tendency became apparent in 1995. Recurrent severe epistaxis lasting for several hours up to 2 days, recurrent bruises, hematomas and gum bleedings persisted throughout 1995, which ultimately resulted in an iron deficiency state in November 1995 (Hb 5.7 mmol/L, ht 0.30, MCV 77 fl, ferritine 6 ug/L). The clinical picture of microvascular circulation disturbances followed by spontaneous mucocutaneous bleeding manifestations was associated with persistently increased high platelets counts between 1200 and 2200 × 109/L (Figure 1) in the context of hypercellular essential thrombocythemia (Figure 2).
Acquired von Willebrand Syndrome
The pronounced increase of platelet count was associated with an acquired von Willebrand syndrome with values for FVIII: C 0.53, VWF: Ag 0.55, VWF: RCo 0.29 and VWF: CB 0.16 U/ml and prolonged Ivy bleeding time (10 to 15 minutes).
A severe epistaxis on November 28, 1995 lasting for several hours stopped immediately after correction of the VWF parameters to normal (VWF: Ag 1.21 U/ml, VWF: RCo 1.14 U/ml, VWF: CB 0.83 U/ml) by substitution of 3000 units Hemate-P (Aventis Behring, Marburg, Germany). Bone marrow biopsy under general anesthesia under correction of VWF parameters by substitution of 3500 units Hemate-P (Aventis Behring, Marburg, Germany) was uneventful and not followed by bleeding complications. Analysis of the VWFmultimers at time of overt hemorrhagic thrombocythemia in November 1995 (platelets 1946 × 109/L, Figure 1) revealed a significant loss of the high-molecular-weight multimers of VWF comparable with type II von Willebrand Disease (Figure 3).
Reduction of platelet count by treatment of hydroxyurea to near normal values between 400 and 600 × 109/L followed by long-term treatment with anagrelide (Figure 1) was associated with no recurrence and absence of bleeding manifestations, correction of plasma levels of VWF: Ag, VWF: RCo and VWF: CB to normal values together with the reappearance of the high molecular-weight VWF multimers (Figure 4).
Diagnosis of JAK2 wild type Thrombocythemia in PMGM
The peripheral blood film showed red cells with slight anisocytosis and microcytosis, a few schistocytes, a few ovalocytes and a sporadic tear drop cell, absence of normoblasts, a normal white blood differential count (metamyelocytes 0.5%, banded forms 1%, segemented granulocytes 52%, basophiles 2.5%, lymphocytes 35% monocytes 6%), and pronounced increase and clumps of platelets. The leucocyte alkaline phosphatase (LAP) score was low 14 (normal score 10-100).
Bone marrow aspirates yielded material with clumps of platelets in two smears and one smear showed normal cellularity with normal erythropoiesis, slightly increased myelopoiesis with normal maturation, and a pronounced increase of enlarged megakaryocytes with large multilobulated nuclei (Figure 2). The iron stain with Prussian blue was negative consistent with the iron deficient state (ferritin 6 ng/ml) due to recurrent bleeding.
Bone marrow biopsy specimens showed a clearly hypercellular bone marrow with a predominant primary megakaryocytic and granulocytic myeloproliferation according to Georgii & Michiels (PMGM)[2,3] and the absence of reticulin or collagen fibers (Figure 2). Noteworthy is the loose to dense clustering of large immature megakaryocytes, their great variations in size with hyperploid nuclei and some naked nuclei. In addition, several megakaryocytes show definite abnormalities of maturation with bulky (bulbous) hyperchromatic nuclei and some disturbances of the nuclear cytoplasmic ratio (Figure 2). These bone marrow findings are consistent with thrombocythemia as the presenting feature of PMGM (Table 2) [2,3,10,11].
The karyotype of the nucleated bone marrow cells was found to be normal 46, XY in 36 analysed cells. Molecular studies using southern blot analysis of extracted DNA revealed the absence of a rearrangement within the bcr on chromosome 22. After two years of treatment with anagrelide the dose to control platelet number could be decreased (Figure 4). Anagrelide could be discontinued at the end of 1997 without significant increase of the platelet counts (Figure 4). There was a slight increase of both hemoglobin and hematocrit from low normal to high normal levels during subsequent follow-up of 12 years (Figure 4). During that period up to 2003 the spleen was not palpable. The JAK2V617F mutation was not detectable in 2006. Further studies on peripheral blood, bone marrow and spleen size after 2006 are not available due to loss of follow-up.
Hemorrhagic thrombocythemia is defined as a clinical syndrome of spontaneous mucocutaneous hemorrhages associated with extremely high platelet counts in patients with thrombocythemia of various myeloproliferative disorders [22-30]. Several reports in adults demonstrate that hemorrhagic thrombocythaemia with very high platelet counts in excess of 1500 to more than 6000 × 109/L is associated with an acquired von Willebrand factor deficiency . The laboratory features of acquired von Willebrand syndrome with spontaneous bleeding symptoms at time of investigation in reported adults with hemorrhagic thrombocythemia are characterized by: A very high platelet count (range 1285 to 5860 × 109/L), a prolonged Ivy or Simplate bleeding time, a normal or near normal factor VIII coagulant activity and VWF antigen (VWF: Ag) concentration, a very low VWF-ristocetine cofactor activity (VWF: RCo) and vWF-collagen binding activity (VWF: CB) and absence of large and some of the intermediate VWF multimers simulating a type II von Willebrand disease . The present study is the first report of a child with a typical clinical picture of hemorrhagic thrombocythemia associated with a well-documented acquired von Willebrand syndrome type 2A. In all adults, reduction of platelet count to near normal resulted in the complete relief of bleeding manifestations, the disappearance of the acquired von Willebrand syndrome, and correction of all VWF parameters to normal with the reappearance of the intermediate and high VWF multimers in plasma (Figure 4) [25-31]. A correct diagnosis in patients with a persistent increase of platelet counts, either asymptomatic or with microvascular thrombotic complication and/or hemorrhagic manifestations, remains a challenge. According to WHO ECMP criteria, bone marrow histopathology appears to be a specific clue to a proper classification and diagnostic differentiation of thrombocythemia in various myeloproliferative disorders [2,32,33]. In reactive thrombocytosis the number of megakaryocytes is increased, but the morphology and size of megakaryocytes remain normal, small and mature and there is no tendency to clustering [2,11,32,33]. In Phpositive ET and in thrombocythemia associated with Ph-positive chronic myeloid leukemia, the megakaryocytes in bone marrow smears and biopsy material are clearly smaller than normal with round nuclei showing minor lobulations . In contrast, both the number and size of megakaryocytes in bone marrow smears and biopsies are typically increased in Ph-negative ET . Enlarged megakaryocytes with mature cytoplasm and multilobulated nuclei and their tendency to cluster in small groups close to sinuses are the hallmark of JAK2V617F ET [2,32,33]. The histological background of hematopoisesis in JAK2V617F ET is featured by large mature pleomorphic megakaryocytes and normal cellularity of erythropoisesis and myelopoisesis [2,32,33]. The megakaryocytes in polycythemia may have a rather pleiomorphic appearance with a wide range of sizes, including small to giant forms, and the characteristic increase and clustering of larged megakaryocytes. Proliferation of erythropoisesis with hyperplasia of dilated sinuses are the diagnostic hallmark of untreated polycythemia vera to distinguish it from secondary reactive polycythemias [2,32-34]. The very characteristic histopahological feature of PMGM3 according to Georgii et al.  is a mixed dual proliferation of increased granulopoesis and megakaryopoesis without reticulin or collagen fibrosis, but dominated by atypical immature giant megakaryocytes, which are conspicuously enlarged due to increase of nuclear as well as cellular size with bulky and irregular, roundish-shaped nuclei [2,32,33]. Pronounced dysmegakaryopoiesis with immature cytoplasm and with the so-called cloud-like nuclei are typical for early fibrotic and fibrotic stages of PMGM [2,3] which are is almost never seen in JAK2V617F ET or polycythemia vera [32,33].