Uveal Diseases

Due ulcere… proprio lì

2026/3 — pag. 155-157 — DOI

Dal rene all'occhio: che cos'è la TINU?

Sapienza GM, Greco M, Cardilicchia M, Lo Scalzo L, Spallino E, Corrado C, Pavone G, Cusumano R, Sapia MC, D'Alessandro MM, Corsello G

2024/26 — pag. 2-2 — DOI

An eight-year-old boy presenting with interstitial nephritis (abdominal pain, microhematuria, glycosuria, proteinuria, elevated urinary beta2-microglobulin levels) was eventually diagnosed with TINU syndrome (tubulointerstitial nephritis associated w...

Pioderma gangrenoso

Angrisani F, Acierno S, Marino A, Chighinzola C, Caporali R, Giani T, Cimaz R.

2022/10 — pag. 627-631 — DOI

Pyoderma gangrenosum (PG) is a rare neutrophilic dermatosis, characterized by unknown aetiology and sterile neutrophilic infiltrate on histological examination, clinically showing recurrent skin ulcers and mostly affecting lower limbs areas. In 2/3 o...

Malattia di Behçet: una sfida per il pediatra

Levantino L, Pastore S, Corona F, Lepore L, Tommasini L.

2022/5 — pag. 289-297 — DOI

Behçet’s disease (BD) is a rare chronic inflammatory condition associated with variable-vessel vasculitis, systemic involvement and relapsing course. It is characterized by a wide clinical heterogeneity, presenting with mucocutaneous, ocular, articul...

A caval donato... guarda anche in bocca!

Gustuti V

2022/5 — pag. 114-114 — DOI

A 15-year-old girl with vulvar ulcers previously attributed to recurrent herpetic infection is presented. Aphthous oral ulcers were also present and the diagnosis of Behçet disease was eventually made....

Una PFAPA che diventa un Behçet

Cafolla C, Iacono A, Guiducci C, Mambelli L, Marchetti F

2021/4 — pag. 226-229 — DOI

PFAPA syndrome (periodic fever, aphthous stomatitis, pharyngitis and cervical adenitis) is the most common periodic fever syndrome in children. The disease appears to cluster in families, but the pathogenesis is unknown. The paper reports the descrip...

Occhio al gatto: la toxoplasmosi retinica

V. Migliarino

2020/4 — pag. 91-91 — DOI

Sarà Behçet? Ovvero, che fine fa l’aftosi ricorrente in Pediatria

G. Beatrice

2019/6 — pag. 131-131

Sindrome di Waardenburg

S. Tajè, M.C. Provero, P. Cianci, A. Selicorni

2019/3 — pag. 185-187

Sindrome TINU: dall’occhio al rene andata e ritorno

L. Cortellazzo Wiel, G. Gortani, S. Pastore, S. Pensiero, M. Pennesi, A. Filpo, E. Valletta, A. Ventura

2019/2 — pag. 103-107

TINU stands for TubuloInterstitial Nephritis and Uveitis syndrome. The effective incidence of the disease is unknown, but it probably still remains largely underestimated. This can be explained by the frequent existence of a time-gap between the oc...

Atlante dermatologico pediatrico alfabetico di Medico e Bambino B

2018/11

Un occhio più piccolo e uno più grande

P. Paganin

2018/4

Sindrome di Waardenburg: descrizione di un caso clinico

V. Carrato, A. Spinelli, I. Bruno

2017/5 — pag. 323-324

Waardenburg syndrome - type 1 (WS1) is an autosomal dominant disease clinically and genetically heterogeneous. It is characterized by non-progressive sensorineural hearing loss of variable degree and anomalous pigmentation of the eyes and the skin ca...

PPI e mal di pancia: andata e ritorno Novità forse utili: Apremilast Novità forse utili: Mongersen Evviva la soluzione fisiologica Sonno sicuro per il lattante Formula magica contro la SIRT Sembrava una Kawasaki, era una artrite sistemica

2015/5 — pag. 281-282

Una mancata cataratta

D. Ferrara, A. Macaluso

2013/2 — pag. 123-124

The case of a six-year-old child with idiopathic uveitis that initially was difficult to diagnose is described. Once the correct diagnosis was made, the little patient was adequately treated with immunosuppressants, which determined the clinical ...

Una mancata cataratta

D. Ferrara, A. Macaluso

2013/2

The case of a six-year-old child with idiopathic uveitis that initially was difficult to diagnose is described. Once the correct diagnosis was made, the little patient was adequately treated with immunosuppressants, which determined the clinical reso...

Due casi di torcicollo non proprio banale

L. Lepore

2012/2 — pag. 127

Quasi cieco all'improvviso

Z. Pietrangiolillo, C. Venturelli, A. De Fanti, L. Cimino, I. D'Aquino, A. Crisafi, F. Monti, C. Ruberto, A. Graffagnino, L. Iughetti, S. Amarri

2012/1

Un'uveite isolata ma non troppo

S. Naviglio

2012/1

Quando il bambino non fissa lo sguardo

E. Rubinato, F. Parentin, G. Gortani, M. Spaccini

2010/6 — pag. 397-398

We report the case of a 2-month-old baby who was brought to our attention because his mother noted that he “doesn’t gaze” as his sister did. The child presented with absence of gazing movement and nistagmus. An ophtalmological evaluation revealed...

Fastidiosi genitali... e solito adolescente stanco

G. Brugnoni, A. Bussolini, S. Franzini, C. Gelso, S. Genoni, L. Guerraggio, A. Tosi, S. Zonca, R. Giorgetti

2008/5

L’uveite nell’artrite idiopatica giovanile

ME. Zannin, et al.

2004/6 — pag. 383-388

Uveitis is a frequent complication of rheumatic diseases, and represents one of the main causes of visual loss in the pediatric age. In 80% of the cases anterior uveitis is associated with juvenile idiopathic arthritis (JIA) and is chronic and asym...

La talidomide

F. Marchetti, A. Lenhardt, M. Lazzerini, Et Al.

2003/8 — pag. 517-523

The Authors provide an overview of thalidomide: mechanism of action, pharmacokinetics, efficacy and safety profile, with particular reference to experiences reported with pediatric patients. The review was carried out using the MEDLINE database for...

Domande e risposte

2003/4 — pag. 259-261

Le manifestazioni cutanee nelle malattie reumatiche infantili

L. Lepore

2000/8 — pag. 505-511

Cutaneous involvement is frequently present in rheumatic disorders. Usually the cutaneous lesions are typical and are useful for the diagnosis. In some cases the cutaneous involvement is present since the beginning (Schoenlein-Henoch purpura, Kawas...

Rash cutaneo e artrite in un bambino di 4 anni

R. Cimaz, F. Falcini

1999/6 — pag. 351-352

Nuovi usi per vecchi farmaci nelle malattie autoimmuni

L. Lepore e coll.

1999/6 — pag. 368-370

Sindrome di Waardenburg e sindrome del primo arco. Uno studio genealogico

1999/4

La malattia di Behçet a esordio nell’età pediatrica: proposta di uno studio multicentricoIl bambino plasmato: errata corrigeOmeopatia: le ragioni del dissensoDisplasia dell’anca: chi ascoltare?Errata corrige: distrofia miotonica

1997/7 — pag. 420-424