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1.
Childs Nerv Syst ; 27(11): 1885-93, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21442270

ABSTRACT

OBJECTS: We aim to evaluate the characteristics of pediatric patients with neurofibromatosis type 1 (NF1) who developed soft tissue sarcomas (STSs) and central nervous system (CNS) tumors that have been followed up in our center. MATERIALS AND METHODS: Medical records of children with NF1 were retrospectively analyzed. RESULTS: There were 78 patients who met at least two diagnostic criteria for NF1. The median age of patients was 10 years (0.5-18), and M/F ratio was 1.3. The prevalance of the optic glioma was 11.5% (n = 9), and one patient with optic glioma also had cystic astrocytoma, one patient had brain stem tumor, and one patient had a CNS tumor (without histopathologic diagnosis). Seven of nine children were ≥ 7 years old at the time of the diagnosis of optic glioma. Visual impairment developed in four patients, and two of them were treated with radiotherapy solely on the basis of evidence of clinical and radiological progression of the tumors. Four patients developed STSs. Two of them had malignant peripheral nerve sheath tumors (MPNST), and the remaining two had bladder rhabdomyosarcoma. Three of the four patients with STSs died with progressive disease. CONCLUSION: The clinical course of malignancy in NF1 is often different from that of similar tumor types in the general population. Careful follow-up in patients with NF1 is required to enable the early diagnosis of malignancies, and the developments of new targeted therapies are needed for improvement of the outcome for patients of this group, especially with MPNST.


Subject(s)
Central Nervous System Neoplasms/epidemiology , Neurofibromatosis 1/complications , Sarcoma/epidemiology , Soft Tissue Neoplasms/epidemiology , Adolescent , Central Nervous System Neoplasms/pathology , Child , Child, Preschool , Disease Progression , Female , Humans , Infant , Male , Neurofibromatosis 1/pathology , Prevalence , Sarcoma/etiology , Sarcoma/pathology , Soft Tissue Neoplasms/etiology , Soft Tissue Neoplasms/pathology
2.
Childs Nerv Syst ; 26(2): 263-6, 2010 Feb.
Article in English | MEDLINE | ID: mdl-19937253

ABSTRACT

BACKGROUND: Atypical teratoid/rhabdoid tumor (ATsRT) is a rare tumor and extremely aggressive embryonal neoplasm of the central nervous system. Brain tumors in infant are suggestive of some oncogenic prenatal factors. CASE PRESENTATION: We report on a case of ATRT in a 4-month-old infant conceived by in vitro fertilization (IVF). Some previous reports have raised a question about the possible relation between IVF and childhood cancer, particularly embryonal tumors. CONCLUSION: Report of such cases may provide some evidence to identify if there is a real association between congenital tumors and IVF.


Subject(s)
Brain Neoplasms/pathology , Diseases in Twins/pathology , Fertilization in Vitro , Rhabdoid Tumor/pathology , Teratoma/pathology , Brain/pathology , Brain/surgery , Brain Neoplasms/etiology , Brain Neoplasms/therapy , Diseases in Twins/etiology , Diseases in Twins/therapy , Fatal Outcome , Female , Humans , Infant , Magnetic Resonance Imaging , Rhabdoid Tumor/etiology , Rhabdoid Tumor/therapy , Teratoma/etiology , Teratoma/therapy , Twins
3.
Childs Nerv Syst ; 25(1): 63-9, 2009 Jan.
Article in English | MEDLINE | ID: mdl-18843494

ABSTRACT

PURPOSE: To evaluate the clinical features and treatment results of the primary paravertebral malignant tumors (PMTs) in our department. METHODS: Medical records of 28 children with primary PMTs treated between 1988-2007 were analyzed retrospectively. RESULTS: Primary PMTs constituted 4.8% of the cancer cases in our department. Tumor diagnoses were mostly neuroblastoma (46.4%) and soft tissue sarcomas (35.7%). These cases presented with pain (64.3%), motor dysfunction (42.8%), sphincter dysfunction (35.7%), palpable mass (32.1%), and sensory deficits (7.1%). All tumors were extradural. Physical examination revealed motor deficits (53.6%), deep tendon reflex alterations (53.6%), sphincter dysfunction (35.7%), pathologic reflexes (25%), abnormal cutaneous reflexes (25%), and sensory deficits (17.8%). Sixteen had cord compression (CC; 13 clinical, three radiological CC). Eleven of them presented with advanced disease. Seven were managed by surgical departments by primary surgery (three unresponsive). Others were managed by pediatric oncology: five with corticosteroids+/-chemotherapy (one unresponsive), one with radiotherapy (RT), and two with surgery for the clinical CC. Surgery was tumor excision in nine, laminectomy in nine, laminotomy in one, and delayed surgery after chemotherapy in two cases. In chemotherapy and surgery groups, there were neurologic sequela associated with the advanced disease at diagnosis in 38% and 37%, respectively. At 3-year median follow-up, nine patients died, 17 are alive (four with neurologic sequela), and two are lost of follow-up. CONCLUSION: Majority of cases presented with advanced disease. Late referral is the major cause of morbidity and mortality. The CC caused by PMTs should be initially managed with corticosteroids +/- chemotherapy to avoid the adverse late effects of RT and surgery.


Subject(s)
Neuroblastoma/therapy , Spinal Cord Neoplasms/therapy , Spinal Neoplasms/therapy , Adolescent , Child , Child, Preschool , Combined Modality Therapy , Disease-Free Survival , Female , Follow-Up Studies , Humans , Infant , Male , Recovery of Function/physiology , Retrospective Studies , Sarcoma/therapy , Treatment Outcome
4.
Pediatr Hematol Oncol ; 25(7): 685-92, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18850482

ABSTRACT

Mesenchymal hamartoma of the liver (MHL) is an uncommon, benign, tumor-like lesion and is usually diagnosed in the first 2 years of life. Its pathogenesis remains unclear. Treatment of choice is radical excision. The authors report a case of solid stromal predominant MHL in a 12-month-old male infant who also had an elevated serum alpha-fetoprotein level. He also had hypospadias, which might represent a spectrum of developmental anomalies. It usually presents as an asymptomatic mass, however, as in the reported case, it may cause several complications due to the compression of surrounding structures. He was successfully treated with total excision of the pedunculated large tumor without any complication.


Subject(s)
Hamartoma/diagnosis , Liver Diseases/diagnosis , alpha-Fetoproteins/analysis , Diagnosis, Differential , Hamartoma/blood , Hamartoma/pathology , Hamartoma/surgery , Humans , Infant , Liver Diseases/blood , Liver Diseases/pathology , Liver Diseases/surgery , Liver Neoplasms/diagnosis , Liver Neoplasms/pathology , Male , Mesoderm/pathology
5.
Pediatr Hematol Oncol ; 25(6): 522-7, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18728971

ABSTRACT

Pilomatricomas are the most common superficial tumors in children, but they are frequently misdiagnosed preoperatively. There are some characteristic features of pilomatricomas that can help clinicians differentiate it from other tumors. The authors report 3 children with head and neck pilomatricomas, one with multiple tumors. They emphasize some clinical features that may help in differential diagnosis to avoid unnecessary investigations before surgical removal.


Subject(s)
Hair Diseases/pathology , Pilomatrixoma/pathology , Skin Neoplasms/pathology , Child , Diagnosis, Differential , Hair Diseases/surgery , Humans , Male , Pilomatrixoma/surgery , Skin Neoplasms/surgery
6.
Pediatr Hematol Oncol ; 25(1): 79-82, 2008.
Article in English | MEDLINE | ID: mdl-18231958

ABSTRACT

Phyllodes tumor (PT) is an uncommon tumor in adolescent girls and young women. A case of PT in a 14-year-old girl is reported. The clinical examination showed a painless tumor that had grown during 10 months. Total excision of the mass with wide margin was performed. The diagnosis, behavior, and treatment of this rare tumor are discussed.


Subject(s)
Breast Neoplasms/pathology , Phyllodes Tumor/pathology , Adolescent , Breast Neoplasms/diagnosis , Breast Neoplasms/surgery , Disease-Free Survival , Epithelial Cells , Female , Humans , Mastectomy, Segmental , Phyllodes Tumor/diagnosis , Phyllodes Tumor/surgery , Stromal Cells
7.
Pediatr Hematol Oncol ; 24(8): 615-21, 2007 Dec.
Article in English | MEDLINE | ID: mdl-18092252

ABSTRACT

Although veno-occlusive disease of the liver is a well-known complication of high-dose chemotherapy and bone marrow transplantation, it has rarely been observed in children who receive conventional chemotherapy. Most cases in the literature consists of children with Wilms tumor. It has been very uncommon in rhabdomyosarcoma patients until recently, although they commonly receive similar anticancer agents. Here the authors report a 2-year-old boy with rhabdomyosarcoma who developed veno-occlusive disease while receiving VAC (vincristine, actinomycin D, cyclophosphamide) chemotherapy regimen according to the IRS-IV protocol. The patient gradually recovered during 2 weeks with supportive treatment only.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/adverse effects , Hepatic Veno-Occlusive Disease/chemically induced , Rhabdomyosarcoma/complications , Rhabdomyosarcoma/drug therapy , Antineoplastic Combined Chemotherapy Protocols/administration & dosage , Bone Marrow Transplantation/adverse effects , Child, Preschool , Cyclophosphamide/administration & dosage , Cyclophosphamide/adverse effects , Dactinomycin/administration & dosage , Dactinomycin/adverse effects , Hepatic Veno-Occlusive Disease/pathology , Hepatic Veno-Occlusive Disease/therapy , Humans , Male , Remission Induction , Vincristine/administration & dosage , Vincristine/adverse effects , Wilms Tumor/complications , Wilms Tumor/therapy
8.
Turk J Pediatr ; 47(3): 279-82, 2005.
Article in English | MEDLINE | ID: mdl-16250317

ABSTRACT

Patients with cancer have an increased risk for thromboembolism, which might be related to several factors including central venous catheters and chemotherapeutics. Congenital prothrombotic risk factors might also contribute to thrombotic events. In this report, we present a catheter-related recurrent intracardiac thrombosis in a boy with non-Hodgkin's lymphoma and factor V Leiden mutation. Screening for factor V Leiden mutation in children with cancer and recurrent thrombotic events is recommended. Periodic echocardiography may be considered for a group of patients if the catheter tip is in the right atrium and therapy includes L-asparaginase and corticosteroids.


Subject(s)
Catheters, Indwelling/adverse effects , Factor V/genetics , Heart Atria/diagnostic imaging , Heart Diseases/etiology , Lymphoma, Non-Hodgkin/complications , Thrombosis/etiology , Child , Humans , Male , Recurrence , Thrombosis/diagnostic imaging , Ultrasonography
9.
Pediatr Hematol Oncol ; 21(6): 535-43, 2004 Sep.
Article in English | MEDLINE | ID: mdl-15552817

ABSTRACT

In this study, 136 febrile neutropenic episodes were overviewed retrospectively. Factors affecting treatment success and cost were analyzed. Twenty percent of the episodes were microbiologically documented and 51 % of the bacterial isolates were gram negatives. The most commonly used empirical therapies in febrile episodes were the combination of two drugs (58.0%), monotherapy (14.8%), and antibiotics plus fluconazole (20.6 %). In lymphoproliferative tumors duration of fever and discharge from the hospital were longer Administration of the hematopoietic growth factors shortened neither the duration of neutropenia nor fever and hospitalization. Treatment costs were higher in lymphoproliferative tumors, in bacteremia, and in episodes where glycopeptides, antifungal drugs, and hematopoietic growth factors were used. In conclusion, duration of neutropenia was a significant independent predictive factor for duration of fever In the lymphoproliferative tumors, duration of fever was longer and cost of treatment was more than in the solid tumors.


Subject(s)
Fever/therapy , Health Care Costs , Neoplasms/complications , Neutropenia/therapy , Adolescent , Child , Child, Preschool , Female , Humans , Infant , Male
10.
J Pediatr Hematol Oncol ; 25(9): 740-2, 2003 Sep.
Article in English | MEDLINE | ID: mdl-12972812

ABSTRACT

Recipients of solid organ allografts are known to be at increased risk of developing Epstein-Barr virus-related posttransplant lymphoproliferative diseases. A 28-month-old boy who had received a heterotopic liver transplant presented with lymphadenopathy in the abdomen, multiple nodules in the liver, and bilateral renal infiltration 19 months after transplantation. He was diagnosed with a Burkitt-like lymphoma based on bone marrow examination and the finding that the blastic cells in bone marrow were EBER-1 positive. Cytogenetic analysis of the bone marrow cells showed an MLL-AF4 rearrangement. He was treated with a combined chemotherapy regimen. He has been in continuous complete remission for 15 months now.


Subject(s)
Epstein-Barr Virus Infections , Immunosuppressive Agents/adverse effects , Liver Transplantation/adverse effects , Lymphoma, B-Cell/genetics , Oncogene Proteins, Fusion/genetics , Tumor Virus Infections , Biliary Atresia/surgery , Child, Preschool , Chromosomes, Human, Pair 11/genetics , Chromosomes, Human, Pair 11/ultrastructure , Chromosomes, Human, Pair 4/genetics , Chromosomes, Human, Pair 4/ultrastructure , Disease Transmission, Infectious , Epstein-Barr Virus Infections/transmission , Humans , Lymphoma, B-Cell/etiology , Lymphoma, B-Cell/virology , Male , Myeloid-Lymphoid Leukemia Protein , Oncogene Proteins, Fusion/analysis , Translocation, Genetic , Tumor Virus Infections/transmission
11.
Pediatr Hematol Oncol ; 19(4): 211-8, 2002 Jun.
Article in English | MEDLINE | ID: mdl-12051586

ABSTRACT

Since a large variety of disorders may lead to lymph node enlargement determining the cause of peripheral lymphadenopathy (LAP) in children can be difficult. This retrospective study evaluated 200 children who were admitted to an Oncology-Hematology department because of lymphadenopathy and aimed to determine the clinical and laboratory findings that were valuable for differential diagnosis. A specific cause for lymphadenopathy was documented in 93 (46.5%) cases. One hundred forty (70%) children were classified as having a benign cause for lymph node enlargements. Fourteen (10%) of these cases underwent an excisional lymph node biopsy, and histopathological examination showed a reactive hyperplasia. Sixty (30%) cases were classified as having a malignant disease-causing lymphadenopathy. In terms of differential diagnosis, some associated systemic symptoms, physical findings, and laboratory investigations showed significant difference between benign and malignant lymphadenopathy groups. The following findings were determined as being important to alert the physician about the probability of a malignant disorder: location of the lymphadenapathy (supraclavicular and posterior auricular), duration of the lymph node enlargement (>4 weeks), size of the lymph node (>3 cm), abnormal complete blood cell findings, abnormalities in chest X-ray, and abdominal ultrasonography.


Subject(s)
Lymph Nodes/pathology , Lymphatic Diseases/diagnosis , Child , Diagnosis, Differential , Hematologic Tests , Hematology , Hospital Departments , Humans , Lymphatic Diseases/etiology , Medical Oncology , Radiography, Thoracic , Retrospective Studies , Turkey
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