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1.
Ital J Pediatr ; 50(1): 7, 2024 Jan 17.
Article En | MEDLINE | ID: mdl-38233867

BACKGROUND: Norwegian scabies is a rare dermatological manifestation that usually affects the most fragile populations, such as elderly and immunocompromised patients, and its diagnosis is quite complex, due to its low prevalence in the general population and because of a broad spectrum manifestation. CASE PRESENTATION: Here we describe a rare case of Norwegian scabies that was previously misdiagnosed in a sixteen year old patient affected by Down syndrome and we conducted a non-systematic literature review about this topic. Lesions were atypical, pruritic and associated with periodic desquamation of the palms and soles and after a series of specialist evaluations, she finally underwent topical treatment with complete remission. CONCLUSION: It is therefore crucial to take in consideration the relation between Down syndrome and community acquired crusted scabies, to enable preventative measures, early detection, and proper treatment.


Down Syndrome , Scabies , Adolescent , Female , Humans , Down Syndrome/complications , Norway , Scabies/diagnosis , Scabies/drug therapy , Scabies/complications
3.
Ital J Pediatr ; 49(1): 61, 2023 Jun 05.
Article En | MEDLINE | ID: mdl-37277843

BACKGROUND: Acute cerebellar ataxia (ACA) and acute cerebellitis represent disorders characterized by a para-infectious, post-infectious, or post-vaccination cerebellar inflammation. They are relatively common neurologic disorders among children, and may follow infections, or, more rarely, vaccinations. Few cases are instead described among infants. Although the immunization with meningococcal group B (MenB) vaccine has been associated with some neurological side effects, suspected ACA has been reported only once in the literature. CASE PRESENTATION: we describe a 7-month-old female that presented ACA within 24 h from the MenB second dose vaccination. Extensive laboratory studies and magnetic resonance imaging excluded other causes. We then conducted an extended review of other vaccine related cases reported in the literature, focusing on the clinical characteristics of ACA and finding that ataxia and cerebellitis of para- or post-infectious cause are very rarely described in the first year of life. We collected 20 articles published in the last 30 years, including an amount of 1663 patients (1-24 years) with ACA. CONCLUSIONS: a very small number of suspected post-vaccinal ataxias has been described in recent years, compared to other causes, and vaccination remains an unquestionable medical need. Further research is needed to clarify the complex pathogenesis of this disorder and its eventual link with vaccinations.


Cerebellar Ataxia , Meningococcal Vaccines , Female , Humans , Infant , Acute Disease , Cerebellar Ataxia/chemically induced , Magnetic Resonance Imaging , Meningococcal Vaccines/adverse effects , Vaccination/adverse effects
4.
Pediatr Dermatol ; 38(5): 1185-1190, 2021 Sep.
Article En | MEDLINE | ID: mdl-34463363

We observed ten children with a papular eruption with purpuric features during the SARS-CoV-2 pandemic in Northern Italy (May-December 2020). Histological examination showed signs of SARS-CoV-2-related dermatosis. Evidence of nucleocapsid viral proteins using SARS-CoV-2 (2019-nCoV) nucleocapsid antibody revealed cuticular staining of the deep portion of the eccrine glands in all cases.


COVID-19 , Dermatitis , Purpura , Humans , Pandemics , Purpura/etiology , SARS-CoV-2
7.
Pediatr Dermatol ; 37(3): 437-440, 2020 May.
Article En | MEDLINE | ID: mdl-32374033

During the COVID-19 pandemic, chilblain-like lesions have been reported in mildly symptomatic children and adolescents. We present four children investigated for suspected COVID-19 infection who presented with acral skin findings and mild systemic symptoms. Histology from one case showed signs of vasculitis with evident fibrin thrombus.


Betacoronavirus , Chilblains/diagnosis , Chilblains/virology , Coronavirus Infections/complications , Coronavirus Infections/pathology , Pneumonia, Viral/complications , Pneumonia, Viral/pathology , COVID-19 , Child , Child, Preschool , Female , Humans , Male , Pandemics , SARS-CoV-2
8.
Lasers Surg Med ; 52(7): 597-603, 2020 09.
Article En | MEDLINE | ID: mdl-31828809

BACKGROUND AND OBJECTIVES: Infantile hemangiomas (IHs) are the most common benign tumors in infanthood. Although they are often self-limiting, management of IHs is still controversial because residual lesions may persist in some cases. The aim of this study is to report our experience with patients affected with IH and investigate the frequency of residual lesions in treated versus untreated patients. STUDY DESIGN/MATERIALS AND METHODS: This retrospective observational study enrolled patients with IHs evaluated over the past 10 years. Patients were managed with systemic or local pharmacotherapy, laser therapy, a combination of them, or with observation only. RESULTS: A total of 432 patients were included: 71% received one or more therapies for IHs; 75.2% of untreated patients had at least one residual lesion compared with 41.4% of treated patients (P < 0.001). Patients treated with laser therapy or topical timolol had the lowest rate of residual lesions. CONCLUSIONS: This rather large case series suggests that IHs management with pharmacotherapy and especially laser therapy is associated with a lower number of residual lesions than observation only. Although propranolol can be very useful to avoid life-threatening complications and severe tissue impairment, laser therapy and topical timolol are potential effective treatments to decrease the incidence of residual lesions, mostly associated with superficial IHs. Lasers Surg. Med. © 2019 Wiley Periodicals, Inc.


Hemangioma, Capillary , Lasers, Dye , Skin Neoplasms , Humans , Infant , Lasers, Dye/therapeutic use , Observational Studies as Topic , Propranolol/therapeutic use , Skin Neoplasms/drug therapy , Timolol/therapeutic use , Treatment Outcome
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