Search results for "PEDIATRIA"

showing 10 items of 692 documents

PARVOVIRUS INFECTION AND KAWASAKI DISEASE: ONE DISEASE FOR TWO SIBLINGS

2018

Introduction: Kawasaki disease (KD) is rarely described in siblings in the same time. In these cases, an infectious trigger must be excluded. Objectives: We describe the clinical course of two brothers who showed severe KD all at once, secondary to Parvovirus infection. Methods: A 9-month-old female showed fever, pallor, vomiting, bilateral non-secreting conjunctivitis, rash. Anamnesis revealed that 12 days before, she had fever, spontaneously resolved. At admission, 9 days after fever onset, she showed fever, conjunctivitis, pharyngitis, rash, and cervical adenopathy. Haematological parameters showed: leukocytosis, neutrophilia; anaemia; CRP: 2.31; ESR: 120. ECG and echocardiography were n…

Settore MED/38 - Pediatria Generale E SpecialisticaPARVOVIRUS INFECTION KAWASAKI DISEASE SIBLINGS
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DUE FRATELLI, IL PARVOVIRUS E DUE KAWASAKI CON FENOTIPO ATIPICO

2018

E' rara la descrizione della Malattia di Kawasaki (MK) in fratelli, ma -se presente- è necessario escludere un trigger infettivo. Riportiamo il caso di due fratelli affetti da MK esordita contemporaneamente in seguito ad un’infezione da Parvovirus. Una bambina di 9 mesi ha presentato febbre, vomito, esantema, congiuntivite non purulenta bilaterale, linfoadenite. All’anamnesi, emergeva un episodio febbrile 12 giorni prima, con risoluzione spontanea in 5 giorni. Presentava: leucocitosi neutrofila, anemia, con transaminasi, Na, albumina, creatinina, urine nella norma. PCR: 2,31 mg/dl; VES: 120. ECG ed ecocardio sono risultati nella norma, con Z-score coronarici normali. IgM anti-Parvovirus era…

Settore MED/38 - Pediatria Generale E SpecialisticaPARVOVIRUS MALATTIA DI KAWASAKI FENOTIPO ATIPICO
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Autoimmune thyroiditis and phenilketonuria: a new association

2011

Settore MED/38 - Pediatria Generale E SpecialisticaPHENILKETONURIAAUTOIMMUNE THYROIDITIS
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Generalized anasarca as way of presentation of severe protein losing enteropathy.

2009

Settore MED/38 - Pediatria Generale E SpecialisticaPLE
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Familial Protein Losing Enteropathy

2006

Settore MED/38 - Pediatria Generale E SpecialisticaPLELymphangectasia
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LO STUDIO DEI POTENZIALI EVOCATI VISIVI E UDITIVI IN PAZIENTI CON MALATTIA DI KAWASAKI: CASISTICA DELLA CLINICA PEDIATRICA DI PALERMO

2018

La Malattia di Kawasaki (MK), una vasculite sistemica con elettivo interessamento coronarico, può portare a complicanze a carico di diversi distretti quali fegato, reni, polmoni, intestino, occhi, cute, SNC. La sordità neurosensoriale è descritta in casi sporadici e può essere persistente. Lo studio dei potenziali evocati uditivi (ABR) e visivi (PEV) è metodica efficace per identificare, in assenza di sintomi uditivi e/o visivi, alterazioni degli stessi. Abbiamo studiato 52 pazienti (31 M; 21 F; età: 3 mesi-10 anni) con MK mediante PEV e ABR, sia in fase acuta di malattia che durante il follow-up ed abbiamo correlato i risultati dei potenziali con i parametri clinici, la forma della MK (tip…

Settore MED/38 - Pediatria Generale E SpecialisticaPOTENZIALI EVOCATI VISIVI POTENZIALI EVOCATI UDITIVI MALATTIA DI KAWASAKI
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DOWN REGULATION OF LYMPHOCYTES APOPTOSIS IN GIRLS WITH PRECOCIOUS PUBERTY

2011

The effects of sexual hormones secretion in children with precocious puberty induce significant somatic and psychological changes, with systemic implications on several organs and tissues. Besides immune system and blood cells are involved in these changes. Recent studies on mice lymphocytes have demonstrated a protection of estrogens against apoptosis Fas-FasL pathway. These data could partially elucidate why autoimmune diseases are more frequent in females adolescents, whereas males have higher mortality associated with infectious diseases. We studied ten girls (age: 4-7 years) affected by idiopathic precocious puberty, with pubertal stage B3-PH3-4. All presented increased bone age/chrono…

Settore MED/38 - Pediatria Generale E SpecialisticaPRECOCIOUS PUBERTYLYMPHOCYTES APOPTOSIS
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ISOLATED PYODERMA GANGRENOSUM AND ADALIMUMAB:CASE REPORT IN PAEDIATRIC AGE

2018

Introduction: Pyoderma Gangrenosum (PG) is a sterile neutrophilic disorder, rarely described in children and adolescents, and frequently it is known as secondary to other chronic inflammatory diseases. However, epidemiological, clinical and therapeutic data on paediatric PG are numerically limited and no randomized controlled trials have been published. Associated diseases in paediatric cases are inflammatory bowel diseases, vasculitis, immune deficiencies, PAPA Syndrome. The treatment with systemic steroids and cyclosporine is well documented in the literature as the first-line treatment. In nonresponders, other treatment lines are indicated, as: corticosteroids and mycophenolate mofetil, …

Settore MED/38 - Pediatria Generale E SpecialisticaPYODERMA GANGRENOSUM ADALIMUMAB NEUTROPHILIC DISORDER
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SOFT TISSUE SARCOMAS: Surgical Results from Italian Spft Tissue Sarcoma Group

1993

The Authors report the experience of the Italian Society of Paediatric Haematology and Oncology (AIEOP) in the treatment of Rhabdomyosarcoma, according to the Protocol ICS-RMS 88, is here reported.

Settore MED/38 - Pediatria Generale E SpecialisticaPaediatric solid tumours sarcoma Italian protocolSettore MED/20 - Chirurgia Pediatrica E Infantile
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Patologia Muscolare Autoimmune: dermatomiosite. La nostra casistica.

2017

Settore MED/38 - Pediatria Generale E SpecialisticaPatologia Muscolare Autoimmune dermatomiosite
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