Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/5533
Title: Lower motor neuron disease associated with myelofibrosis
Authors: Bir, Levent Sinan
Keskin, Ali
Yaren, Arzu
Sermez, Yurdaer
Oğuzhanoğlu, Attila
Şahiner, Türker
Keywords: Haematological malignancies
Lower motor neuron syndrome
Motor neuron diseases
Myelofibrosis
Myeloproliferative diseases
Paraneoplastic syndrome
hydroxyurea
phenytoin
adult
article
bone marrow biopsy
bone marrow cell
bone marrow culture
case report
cell density
computer assisted tomography
disease association
electromyography
fasciculation
forearm
hepatomegaly
human
larynx disorder
male
megakaryocyte
motor neuron disease
motor unit potential
muscle atrophy
muscle cramp
muscle fiber membrane potential
muscle weakness
myelofibrosis
myeloproliferative disorder
neck
nerve conduction
neurologic examination
nuclear magnetic resonance imaging
palate
paraneoplastic syndrome
splenomegaly
tendon reflex
Atrophy
Humans
Male
Middle Aged
Motor Neuron Disease
Muscle, Skeletal
Abstract: We present a patient who has signs pointing to the involvement of lower motor neurons and myelofibrosis. To our knowledge, unlike lymphoproliferative disorders, co-occurrence of myelofibrosis and lower motor neuron disease (MND) has not been reported so far. A 64-year-old male patient was admitted to our hospital with the complaint of painful cramps in his neck and forearms. On physical examination marked hepatomegaly and splenomegaly were found. On neurologic examination nasal quality of the voice and slight palatal weakness were detected. There were generalised slight weakness and atrophy in both proximal and distal muscle groups. Fasciculations were observed especially in forearm muscles and it was observed that he had been avoiding head movements because of painful muscle cramps. Deep tendon reflexes were hypoactive. Nerve conduction studies were normal. By needle electromyography, giant motor unit action potentials (amplitudes up to 8 mV), fibrillation potentials, positive sharp waves and fasciculation potentials were detected in all muscles which were investigated. A hypercellular bone marrow (100%) was determined by bone marrow biopsy. In addition to increased production of the myeloid and megakaryocytic lines, abnormal aggregation and grouping of megakaryocytes were seen. Reticular fibers were increased. He had some benefit of dyphenilhydantoin treatment given for the painful cramps in his neck and forearm muscles. Hydroxyurea treatment was started for myelofibrosis. Six months later, his general condition was better, and the painful cramps were completely resolved. No marked deterioration has been detected in neurologic examination and electromyography for 1 year. Copyright (C) 2000 Elsevier Science B.V.
URI: https://hdl.handle.net/11499/5533
https://doi.org/10.1016/S0303-8467(00)00072-X
ISSN: 0303-8467
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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