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1.
Sci Total Environ ; 948: 174697, 2024 Jul 15.
Article in English | MEDLINE | ID: mdl-39019280

ABSTRACT

The fate of black biodegradable mulch film (MF) based on starch and poly(butylene-adipate-co-terephthalate) (PBAT) in agricultural soil is investigated herein. Pristine (BIO-0) and UV-aged film samples (BIO-A192) were buried for 16 months at an experimental field in southern Italy. Visual, physical, chemical, morphological, and mechanical analyses were carried out before and after samples burial. Film residues in the form of macro- and microplastics in soil were analyzed at the end of the trial. Progressive deterioration of both pristine and UV-aged samples, with surface loss and alterations in mechanical properties, occurred from 42 days of burial. After 478 days, the apparent surface of BIO-0 and BIO-A192 films decreased by 57 % and 66 %, respectively. Burial determined a rapid depletion of starch from the polymeric blend, especially for the BIO-A192, while the degradation of the polyester phase was slower. Upon burial, an enrichment of aromatic moieties of PBAT in the film residues was observed, as well as microplastics release to soil. The analysis of the MF degradation products extracted from soil (0.006-0.008 % by mass in the soil samples) revealed the predominant presence of adipate moieties. After 478 days of burial, about 23 % and 17 % of the initial amount of BIO-0 and BIO-A192, respectively, were extracted from the soil. This comprehensive study underscores the complexity of biodegradation phenomena that involve the new generation of mulch films in the field. The different biodegradability of the polymeric components, the climate, and the soil conditions that did not strictly meet the parameters required for the standard test method devised for MFs, have significantly influenced their degradation rate. This finding further emphasizes the importance of implementing field experiments to accurately assess the real effects of biodegradable MFs on soil health and overall agroecosystem sustainability.

2.
Int J Infect Dis ; 14(2): e167-70, 2010 Feb.
Article in English | MEDLINE | ID: mdl-19880337

ABSTRACT

Disseminated disease caused by non-tuberculous, environmental mycobacteria (EM) reflects impaired host immunity. Disseminated disease caused by Mycobacterium scrofulaceum has primarily been reported in patients with AIDS. Moreover, observing M. scrofulaceum as the agent of localized disease in childhood has become increasingly rare. We report the first case of disseminated disease caused by M. scrofulaceum in a child with inherited interferon-gamma receptor 1 (IFN-gammaR1) complete deficiency. As in this case, mycobacterial bone infections in IFN-gammaR1 deficiency can sometimes mimic the clinical picture of chronic recurrent multifocal osteomyelitis.


Subject(s)
Immunologic Deficiency Syndromes/complications , Mycobacterium Infections, Nontuberculous , Mycobacterium scrofulaceum/isolation & purification , Receptors, Interferon/deficiency , Tuberculosis, Osteoarticular , Child, Preschool , Foot/microbiology , Foot/pathology , Hand/microbiology , Hand/pathology , Humans , Leg/microbiology , Leg/pathology , Male , Mycobacterium Infections, Nontuberculous/microbiology , Mycobacterium Infections, Nontuberculous/pathology , Tuberculosis, Osteoarticular/microbiology , Tuberculosis, Osteoarticular/pathology , Interferon gamma Receptor
3.
Pediatr Blood Cancer ; 50(2): 413-5, 2008 Feb.
Article in English | MEDLINE | ID: mdl-16835906

ABSTRACT

Chromophobe renal cell carcinoma (CRCC) is a distinct variant of renal carcinoma generally affecting adults. We report a case of an unusual CRCC, arising in a male child affected by hypospadias. This case demonstrates that CRCC can occur in the pediatric patients and can be associated with genital tract anomalies such as Wilms tumor.


Subject(s)
Carcinoma, Renal Cell/complications , Eosinophilia/pathology , Hypospadias/complications , Kidney Neoplasms/complications , Carcinoma, Renal Cell/pathology , Child , Humans , Hypospadias/pathology , Kidney Neoplasms/pathology , Male
5.
Pediatr Radiol ; 32(8): 552-5, 2002 Aug.
Article in English | MEDLINE | ID: mdl-12136344

ABSTRACT

We describe the US findings in two vomiting newborns affected by different forms of pyloric atresia, a rare congenital anomaly that includes a spectrum of lesions limited to the antro-pyloric region of the stomach and with various inheritance mechanisms and syndromic associations.


Subject(s)
Epidermolysis Bullosa/complications , Intestines/abnormalities , Pylorus/abnormalities , Female , Humans , Infant, Newborn , Pylorus/diagnostic imaging , Ultrasonography
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