Skull

C’era una volta un bernoccolo…

Da Lozzo P.

2022/2 — pag. 130 — DOI

An 8-year-old boy presenting with a long-standing cranial bumps was eventually diagnosed with bone fibrodysplasia. The clinical features of this condition and its possible association with McCune-Albright syndrome are discussed. ...

C’era una volta un bernoccolo…

Da Lozzo P

2022/2 — pag. 56-56 — DOI

An 8-year-old boy presenting with a long-standing cranial bumps was eventually diagnosed with bone fibrodysplasia. The clinical features of this condition and its possible association with McCune-Albright syndrome are discussed. ...

“Klingon baby”: quando il sole fa male alla testa

Imperatore A, Brienza C, Porto A, Nunziata F

2021/10 — pag. 314-315 — DOI

The paper describes the case of a 4-year-old boy who presented with sudden head swelling. Clinical findings sustained the diagnosis of “sunburn of the scalp with subsequent oedema of the cutis adjoining the galeal aponeurosis”. Pathogenesis, differen...

Foramina parietalia permagna: descrizione di un caso clinico e revisione della letteratura

Mazzoni S, Guidi B, Tavani F

2021/2 — pag. 51-54 — DOI

The purpose of the present work is to expose the defects of parietal bone ossification and to identify the criteria for differential diagnosis and brain changes related to the condition, with particular attention to the venous developmental anomalies...

Un caso di zoppia: l’istiocitosi a cellule di Langerhans

C. Pizza, G. Trippella, I. Maccora, E. Sieni

2019/10 — pag. 249-249

Inspiegabili bernoccoli

M.C. Pellegrin, A. Delise, D. Sanabor, E. Faleschini, I. Bruno

2015/3

Fibrous dysplasia (FD) is a nonhereditary benign condition in which medullary bone is replaced by immature bone and fibrous tissue. It accounts for 7% of all benign bone tumours and usually presents in the first three decades of life. FD arises f...

Un vero grattacapo

A. Pirrone

2013/6

Depressione congenita del cranio nel neonato: presentazione di un caso clinico

D. Bove, N. De Paulis, M. Giorgino, G. Pepe, A. Seccia

2010/6

Teste piccole, teste grandi, teste storte

L. Genitori, F. Giordano, F. Mussa, M. Sanzo, L. Sardo, G. Di Pietro, P. Donati

2007/3 — pag. 155-159

The right and early diagnosis of craniosynostosis is a mainstay in their surgical management. The Pediatrician often makes the first medical examination of a child with a suspected craniofacial malformation. The aim of this paper is describing the f...

Miofibromatosi congenita

I. Marinelli, A. Vendemiati, C. Fiorentini, F. Arcangeli

2001/10 — pag. 697-697

Congenital myofibromatosis can be cutaneous or visceral. Report of a case featuring multiple elements, both endophytic and exophytic, which appeared after birth and spontaneously regressed. One of them was accompanied by a lack in cranial bones....

Le craniosinostosi, viste dal pediatra

G. Bartolozzi, P.A. Donati

1999/1