Posters, 5th International Congress on Pediatric MDS and Bone ...

<strong>Posters</strong>, <strong>5th</strong> <strong>International</strong> <strong>Congress</strong> on Pediatric MDS and Bone Marrow Failure Syndromes 2009, Rotterdam
Nr. AUTHORS TITLE
PO-01 Concetta Micalizzi, Johanna Svahn, Francesca Scuderi, Tiziana Lanza, Maura Faraci,
Laura Banov, Michaela Calvillo, Oriana Burlando, Francesca Fioredda, Daniela Caprino,
Carlo Dufour.
Chronic urticaria as first sign of MDS
PO-02 Noha M.El Hossainy(1)Mervat M. Mattar (2) prohepcidin in myelodysplasia
PO-03 *A Piccin,^U Rovigatti,*C Mc Mahon,#J Kelly,##B Bourke,*A OíMarcaigh,*OP Smith THIOPURINE S-METHYL TRANSFERASE POLYMORPHIC STATUS, 6-MERCAPTOPURINE, AND
TNF-ALPHA ANTAGONISM IN THE DEVELOPMENT OF MYELODYSPLASTIC SYNDROME /
MONOSOMY 7 IN A CHILD WITH CROHN'S DISEASE
PO-04 Valizadeh,Nasim Myelodysplastic syndrome(MDS) as an early manifestation of Fanconi anemia
PO-05 Rekha Chaubey ,Sudha Sazawal , Manoranjan Mahapatra ,Renu Saxena RAS and FLT3-ITD gene mutations in patients with Myelodysplastic Syndromes in India: AIIMS
experience
PO-06 Shaoyan Hu1* Weiying Gu2 Hailong He1 Yihuan Chai1 Shaoyan Hu and Weiying Gu The features of 65 Chinese pediatric patients with de novo myelodysplastic syndromes
PO-07 Nao Yoshida 1), Hiroshi Yagasaki 2), Yoshiyuki Kosaka 3), Ryoji Kobayashi 4),
Hiromasa Yabe 5), Takashi Kaneko 6), Masahiro Tsuchida 7), Akira Ohara 8),
Tatsutoshi Nakahata 9), Seiji Kojima 2)
PO-08 MuÒoz-Villa A , Diaz de Heredia , Diaz MA , Badell I , Martinez A , Gonzalez-Valentin M
, Dasi MA . Gomez P ,Bureo E , Olive T , Perez-Hurtado JM , Vicent MG and Maldonado
MS on behalf of GETMON
Predicting response to immunosuppressive therapy in childhood aplastic anemia
Very severe acquired aplastic anemia: historical outcome of patients treated by allogeneic bone
marrow transplantation from matched sibling donors. A study by the Spanish Group for Blood
and Marrow Transplantation in Children (GETMON)
PO-09 Masafumi Ito, Ryoichi Ichihashi, Masahiko Fujino, Seiji Kojima* Absence of Hemoglobin F expression on bone marrow erythroblasts identifies a distinct subset
of acquired aplastic anemia patients with good response to immunosuppressive therapy
PO-10 Ferrara M., Capozzi L., Russo R. INCIDENCE OF MALIGNANCY IN A FAMILY OF A PATIENT WITH FANCONI ANAEMIA (FA)
PO-11 Perolla.A , Caja.T, Xhumari.P , Pulluqi.P , Pushi. A PANCYTOPENIA- First expression of several blood diseases [ a 10 years study ]
PO-12 M.Sukova(1),E.Mejstrikova(2),S.Pekova(3),J.Cermak(4),D.Pospisilova(5),J.Stary(1) Childhood paroxysmal nocturnal hemoglobinuria/aplastic anemia (PNH/AA) syndrome - analysis
for PNH clonal evolution after immunosuppressive therapy
PO-13 Isabelle Meyts, Marleen Renard, Johan Maertens*, Ann Uyttebroeck Salvage allogeneic stem cell transplantation in a child with severe aplastic anemia in the course
of life-threatening potential invasive fungal lung infection with peri- and myocardial infiltration
PO-14 RAHIM F 1,2,PANAHI M 3,RASHIDI I4 Incidence of Aplastic Anaemia in Khuzestan Province, Iran: A Retrospective Single-Centre Study
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<strong>Posters</strong>, <strong>5th</strong> <strong>International</strong> <strong>Congress</strong> on Pediatric MDS and Bone Marrow Failure Syndromes 2009, Rotterdam
Nr. AUTHORS TITLE
PO-15 Veronica M.E. Neefjes(1), Rienk Y.J. Tamminga(2) ATG IN ACQUIRED APLASTIC ANAEMIA; IS LESS MORE?
PO-16 Pallota, Ronald 1; Gomes, LaÌs 1 Aplastic Anemia secondary to Dengue virus infection: A Case Report
PO-17 Vallero S, Quarello P, Lorenzati A, Renga D, Rivetti E, Laudati R, Farinasso L, Timeus F,
Ramenghi U, Saracco P
PO-18 Dr. Maitreyee Bhattacharyya, Dr. Seema Tyagi, Dr. M Mahapatra, Dr. V.P. Chaudhury,
Dr. Renu Saxena
PO-19 F Timeus, N Crescenzio, P Quarello, A Doria, L Foglia, S Pagliano, A Lorenzati, S
Vallero, L Farinasso, P Saracco.
PO-20 Saracco P, Quarello P, Iori AP, Zecca M, Longoni D, Svahn J, Varotto S, Del Vecchio
GC, Dufour C, Ramenghi U, Bacigalupo A, Locasciulli A; Bone Marrow Failure Study
Group of the AIEOP
PO-21 1 Mahfuzah Mohamed, 1 Eni Juraida A. Rahman, 2 Bina S Menon, 1 Caroline Ho, 1
Raja Khuzaiah, 1 Zulaiha Muda, 1 Ida Shahnaz Othman, 1 Lim Yin Sear, 1 Asohan
Thevarajah, 1 Aisyah M. Rivai, 1 Hishamshah M. Ibrahim
Use of pegylated granulocyte-colony stimulating factor (PG-CSF) in childhood severe aplastic
anemia.
Etiopathogenesis of childhood aplasticc anemia -- a single center study of 94 cases.
Paroxysmal nocturnal hemoglobinuria clones in children with acquired aplastic anemia: a single
centre study.
Cyclosporin A response and dependence in children with acquired aplastic anaemia: an update
of a multicentre retrospective study with long-term observation follow-up.
Immunosupresstion therapy in children with severe aplastic anaemia
PO-22 Karolien Beel1, Melanie M. Cotter2, Peter Vandenberghe1 Is the risk of developing AML or MDS increased in X-linked neutropenia ?
PO-23 Albert Catala; Susana Rives; Teresa Toll; Mireia CamÛs; Ruben Berrueco; Nuria
Conde; Ana Quintero; JI Arostegui*; Jes˙s Estella
PO-24 M.B. Bierings2, S.N. van der Crabben1, E. van Binsbergen1, M.G.E.M. Ausems1and A.
Buijs1
PO-25 Dr. Maitreyee Bhattacharyya, Dr. Seema Tyagi, Dr. Manoranjan Mahapatra, Dr. V.P.
Chaudhury, Dr. Renu Saxena
PO-26 Tim Ripperger (+), Doris Steinemann (+), Gudrun Gˆhring (+), Charlotte Niemeyer
(*), Brigitte Strahm (*), and Brigitte Schlegelberger (+)
PO-27 Daisuke Hasegawa, Chitose Ogawa, Shinsuke Hirabayashi, Myoung-ja Park, Yasuhide
Hayashi, Atsushi Manabe, Ryota Hosoya.
PO-28 Yoshitoshi Ohtsuka, Mayumi Sugita, Yuka Nakajima, Junichiro Ono, Noriaki Okamoto,
Yuichi Yokokawa, Hiroshi Yoneyama, Takashi Kaneko, Takakuni Tanizawa.
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IMPROVING CONGENITAL NEUTROPENIA DIAGNOSIS: MUTATIONAL ANALYSIS OF ELA2 AND
HAX1 GENES. A SINGLE CENTRE EXPERIENCE
Non-syndromic constitutional RUNX1 deletion presenting as thrombocytopenia with
myelodysplasia.
Childhood aplastic anemia in search for inherited status.
A further pedigree with germline RUNX1 mutation and propensity to myeloid malignancies
A Japanese pedigree with RUNX1 mutation resulting in familial platelet disorder with propensity
to acute myelogenous leukemia (FPD/AML)
Successful unrelated bone marrow transplantation for two patients with amegakaryocytic
thrombocytopenia with radio-ulnar synostosis in Japan.

<strong>Posters</strong>, <strong>5th</strong> <strong>International</strong> <strong>Congress</strong> on Pediatric MDS and Bone Marrow Failure Syndromes 2009, Rotterdam
Nr. AUTHORS TITLE
PO-29 Ferrara M., Capozzi L., Russo R. A case of Congenital Dyserythropoietic Anemia type II (CDA II)
PO-30 I. Furlan, U. Graubner, A. Karow, C. P. Kratz, C.M. Niemeyer Liver fibrosis and telomere maintenance: a family with dyskeratosis congenita
PO-31 1Hashmi SK, 1Allen C, 2Klaassen R, 3Fernandez CV, 4Yanofsky R, 5Wu J,
6Champagne J, 7Silva M, 8Lipton JH, 9Brossard J, 10Samson Y, 11Abish S, 12Steele
M, 13Ali K, 14Dower N, 15Athale U, 16Jardine L, 17Hand JP, 13Beyene J, 1Dror Y
PO-32 Segbefia C, Klaassen R, Fernandez CV, Yanofsky R, Sherek E, Champagne J, Silva M,
Lipton JH, Brossard J, Samson Y, Abish S, Steele M, Ali K, Dower N, Athale U, Jardine
L, Hand JP, Allen C, Beyene J, Dror Y
PO-33 BenoÓte Perez (1,2), Julie Lachenaud (1,2), Sabrina Pereira(1), Marie Laurence
Menot(2), CÈline Liger(1), Fabien Zassadowski(2), Corinne Alberti(3), Christine
Chomienne(2), Bruno Cassinat(2), HÈlËne CavÈ(1,2).
PO-34 Vallero S, Aschero S, Garbarini L, Mazzone R, Crescenzio N, Iavarone A, Ricotti E,
Vassallo E, Nesi F, Cordero di Montezemolo L, Farinasso L
PO-35 A.C.H. de Vries (1), R.G.M. Bredius (2), A.C. Lankester (2), M. Bierings (3), M. Trebo
(4), P. Sedlacek (5), C.M. Niemeyer (6), M. Zecca (7), F. Locatelli (7), M.M. van den
Heuvel-Eibrink (1)
PO-36 Miharu Yabe, Atsushi Manabe, Yoshitoshi Ohtsuka, Kenichirou Watanabe, Masaru
Imamura, Makoto Kaneda, Ryousuke Miyachi, Jirou Inagaki, Yasuhiro Ebihara, Nao
Yoshida, Kazuo Sakashita, Keizo Horibe, Masahito Tsurusawa
COMPARATIVE ANALYSIS OF SHWACHMAN-DIAMOND SYNDROME TO OTHER INHERITED
MARROW FAILURE SYNDROMES
MALIGNANT MYELOID TRANSFORMATION IN INHERITED BONE MARROW FAILURE SYNDROMES
NRAS, KRAS, PTPN11 and NF1 mutations lead to in vitro and clinical differences in Juvenile
Myelomonocytic Leukemia (JMML)
Del(5q) in a patient with JMML, neurofibromatosis 1 and Parvovirus B19 infection.
HLA-IDENTICAL UMBILICAL CORD BLOOD TRANSPLANTATION FROM A SIBLING DONOR IN
JUVENILE MYELOMONOCYTIC LEUKEMIA
Allogeneic hematopoietic stem cell transplantation with fludarabine-containing regimen in
children with juvenile myelomonocytic leukemia
PO-37 Christine Dahl(1), Gitte B. Kerndrup (2), Jan Stary (3), Henrik Hasle (1) Expression of p53 in myelodysplastic syndrome, JMML and non-neoplastic bone marrow failures
in children.
PO-38 Arzu Akyay*, Lale Olcay*, Mehmet Ertem**, I nsu Kuzu**, Nazan Bozdo an*, Elif ‹nal
nce**, Talia leri**, Bet¸l Tavil*, Ay e Say l **, Z¸mr¸t Uysal**
A CASE OF MYELODYSPLASTIC SYNDROME WITH HYPOCELLULER FIBROSIS
PO-39 Maria Helena Ornellas1,2, Mercia Mendes Campos2 Claudia Diniz Athaide2, Bernadete IMMUNOPHENOTYPIC PROFILE IN PEDIATRIC PATIENTS WITH MYELODYSPLASTIC SYNDROME
Evangelho Gomes2,Karen Wagner-Souza2, Teresa de Souza Fernandez1,2 Hilda Rachel IN RIO DE JANEIRO, BRAZIL
Diamond2
PO-40 Roos J Leguit, Marrie CA Bruin, Marc B Bierings, Jan G van den Tweel The pathological findings and survival in pediatric bone marrow failure syndromes. A single
centre review
PO-41 Rinaldi CR 1, Rinaldi P 1, Martinelli V 1, Ciancia R 1, Gugliotta L 2, Vannucchi AM 3,
Barbui T 4, Rotoli B 1 and Pane F 1.
PO-42 Shinsuke Hirabayashi, Keitaro Arima, Takahiro Kamiya, Daisuke Hasegawa, Chitose
Ogawa, Atsushi Manabe, Ryota Hosoya, Etsuro Ito*
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JAK2 V617F mutation in Acute Myeloid Leukemia Secondary to Ph negative Chronic
Myeloproliferative Disorders
Congenital myeloproliferative disease (MPD) with GATA-1 mutation in a phenotypically normal
infant

<strong>Posters</strong>, <strong>5th</strong> <strong>International</strong> <strong>Congress</strong> on Pediatric MDS and Bone Marrow Failure Syndromes 2009, Rotterdam
Nr. AUTHORS TITLE
PO-43 Sudha Sazawal, Jyoti Bajaj, Bharti Sharma, Rahul Bhargava, Rekha Chaubey,
Manoranjan Mahapatra, Renu Saxena
PO-44 Dagmar Pospisilova1, Monika Horvathova2, Jitka Veselovska2, Renata Solna2, Jana
Kucerova2, Jan Stary3, Kveta Petrtylova3, Sona Pekova4, Vladimir Divoky2
PO-45 Janda A.(1), Cermak J.(2), Petrtylova K.(3), Cerna Z.(4), Zemanova Z.(5), Markova
M.(2), Mejstrikova E.(1), Smisek P.(1), Stary J.(1)
PO-46 Laurent Garderet 1,2,3, Ladan Kobari 1,2, Christelle Mazurier 1,4, Caroline De Witte
1,2, Marie-Catherine Giarratana 1,2, Christine PÈrot 5, HÈlËne Lapillonne 1,2,6 & Luc
Douay 1,2,4,6
PO-47 Per O. Iversen (1,2), Elvira Semaeva (3), Dag R. Sorensen (4), Helge Wiig (3) and
Mouldy Sioud (5)
Frequency of JAK2 V617F in Indian patients with Chronic myeloproliferative disorders: AIIMS
experience
ESSENTIAL THROMBOCYTHAEMIA IN CHILDREN: CLINICAL AND LABORATORY
CHARACTERISTICS
Cytopenia progressing slowly towards full-blown MDS-RC, three case reports.
Myelodysplastic 5q(del) clones are able to reach terminal differentiation into enucleated red
blood cells.
A combined immunostimulatory and immunoinhibitory siRNA with anti-leukemic properties in a
rat model of acute myeloid leukemia
PO-48 Yang-Ping Niu, Xu-Dai Qian, Jun-Qing Qian PROLIFERATIVE EFFECTS OF GPD AND GPT ON HUMAN BONE MARROW HAEMOPOIETIC
PROGENITOR CELLS
PO-49 Bing Han, Juan xiao, Yongji Wu, Yuping Zhong, Wanling Sun Ex vivo expansion and hematopoietic reconstitution ability of isolated CD34+CD59+ cells from
patients with paroxysmal nocturnal hemoglobinuria
PO-50 S. Lie Fong, M.D. (1), J.S.E. Laven, Ph.D. (1), F.G.A.J. Hakvoort-Cammel, M.D. (2), I.
Schipper, Ph.D. (1), J.A. Visser, Ph.D. (3), A.P.N. Themmen, Ph.D. (3), F.H. de Jong,
Ph.D. (3), M.M. van den Heuvel - Eibrink, Ph.D. (2).
PO-51 D.Woijcik1,2,J.Musia 1,E.Gorczy ska1,M.Ussowicz1,A.Dyla1,J.Owoc-Lempach1,M. S
ociak1,D.Sega-Pondel1,W.Pietras1 and K.Ka wak1
PO-52 Igor Resnick, Polina Stepensky, Michael Weintraub, Dani Engelhard, Diana Averbukh,
Jacqueline Feinberg, StÈphanie Boisson-Dupuis, Jacinta Bustamante, Jean-Laurent
Casanova.
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Gonadal damage in female adult childhood cancer survivors after total body irradiation,
assessed by anti-M¸llerian hormone
Haematopoietic Stem Cell Transplantation (HSCT) for pediatric MDS-Single center study-
A NOVEL FORM OF MYELODYSPLASTIC SYNDROME (MDS) ASSOCIATED WITH MENDELIAN
SUSCEPTIBILITY TO MYCOBACTERIAL DISEASE (MSMD).