11 research outputs found

    Control of bracken ( Pteridium aquilinum

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    The diminution of pastoral activities in marginal areas, and consequently of livestock grazing, implies a strong encroachment of invasive vegetation. The conservation of the open areas is however particularly important for wildlife management. With this aim, this paper describes the results obtained in a protected area on the Apennine mountains (Italy), encroached by Pteridium aquilinum (L.) Kuhn. Two restoration practices were carried out by the Administration of the Regional Park of the Laghi di Suviana e Brasimone (Bologna, Italy), in order to reverse the infestation of bracken and restore pastures within the park. The pasture, only grazed by wild animals, was improved through different treatments (ploughing followed by cuttings vs harrowing), each followed by seeding of a forage mixture. Our results showed better performance of the ploughing both as pastoral value of recovered pasture and as botanical composition. Some differences in the effects of the two restoration techniques were also found on the biodiversity index and on floristic richness. Data about grazing selection of the single botanical species have also been collected. The tesults also showed different behaviour in feeding preferences for wild ungulates in comparison to domestic stocks, giving a better evaluation of the real forage availability for wild herbivores

    An incidental rectal neuroendocrine microcarcinoma (‘micro-NEC’) coexistent with a high grade adenoma

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    A 72‐year‐old man came to the attention of the clinicians with a long history of diarrhea. The gastroenterologist performed a colonoscopy that revealed diverticular disease in colon and sigma and the presence of an exophytic lesion measuring 4 cm, located at 12 cm from the anals margin and that was biopsied. Histologically, it was a tubulo‐villous adenoma with low grade dysplasia. Computed tomography (CT) scan confirmed the diverticular disease but not the exophytic lesion of the rectum that was evident, instead, on magnetic resonance imaging of the abdomen. No lymph nodes adenomegalies were evident. The patient's medical history did not include any other pathology. A week later, the lesion was removed endoscopically with diathermic loop. Numerous fragments, measuring 5 × 4 cm, were examined. It was concluded that, in the context of a rectal tubulovillous adenoma with high grade dysplasia, a neuroendocrine ‘microcarcinoma’ was detected, that was confined to the mucosa. In the present case the diagnosis was made just by chance, because the adenomatous lesion was voluminous and it had caused diarrhea

    Amyloidoma of the Tongue: Case Report, Surgical Management, and Review of the Literature

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    Purpose: Localized amyloidosis of the tongue is a benign condition in which surgical management may be considered. The aim of the study was to review the current literature and report a case. Materials and Methods: We searched the PubMed database for all relevant articles reporting cases of localized tongue amyloidosis published between 1980 and February 2020. In addition, we updated 1 case diagnosed and treated in our department. Results: A 49-year-old male patient presented with an asymptomatic tongue nodule of the dorsum mimicking median rhomboid glossitis. The results of an incisional biopsy showed an amyloid on Congo red staining and positive findings for the κ light chain by immunohistochemical analysis. The findings of the systemic workup were negative. Therefore, a diagnosis of localized κ light-chain amyloidosis was made. The patient underwent a resection of the lesion, and no recurrence or progression was observed during a period of 18 months. The literature review showed 12 reports describing 21 patients (11 men, 52.3%) with localized tongue amyloidosis. The most common clinical presentation was nodular with a single lesion of the tongue dorsum (15 patients, 71.4%). All cases showed positive findings on Congo red staining. Immunohistochemical analysis findings were available for only 9 patients (42.8%) and showed light-chain amyloidosis. No case showed any systemic involvement or the development of systemic disease. Surgical excision was performed in 9 cases, with recurrence at the site of operation in 2 cases. Conclusions: Localized amyloidosis of the tongue is a rare disease in which surgical excision may be therapeutic when a multidisciplinary evaluation does not show any systemic disease. We recommend an excision when the lesion is persistent or shows an enlargement or when discomfort is reported. In the case of any further local recurrence, resection may be repeated

    Clinical phenotype of lathosterolosis.

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    Lathosterolosis (LS) is a defect of cholesterol biosynthesis due to the deficiency of the enzyme sterol-C5-desaturase. Only two patients have been described to date, both presenting with multiple malformations, mental retardation, and liver involvement. In addition in one of them pathological examination revealed mucolipidosis-like inclusions on optic microscopy analysis, and peculiar lysosomal lamellar bodies on electron microscopy analysis. This study is focused on a better characterization of the clinical phenotype of LS. We describe a further case in a fetus, sibling of the first patient reported, presenting with neural tube defect, craniofacial and limb anomalies, and prenatal liver involvement. The fetal phenotype suggests the possible occurrence of significant intrafamilial variability in LS, and expands the phenotypic spectrum of the disease. Histological examination of autopsy samples from the fetus and skin fibroblasts from the living sibling suggested that the mucolipidosis-like picture previously reported is not a constant feature of LS, being possibly associated with the most severe biochemical defects, but confirmed the ultrastructural finding of lamellar inclusions. The LS phenotype appears to be characterized by the distinctive association of a recognizable pattern of congenital anomalies, involving axial and appendicular skeleton, liver, central nervous and urogenital systems, and lysosomal storage. This condition partially overlaps with other defects of sterol metabolism, suggesting intriguing pathogenic links among these conditions

    Stabilizing electromagnons in CuO under pressure

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    International audienceAbstract Electromagnons (Electroactive spin wave excitations) could prove to be decisive in information technologies but they remain fragile quantum objects, mainly existing at low temperatures. Any future technological application requires overcoming these two limitations. By means of synchrotron radiation infrared spectroscopy performed in the THz energy range and under hydrostatic pressure, we tracked the electromagnon in the cupric oxide CuO, despite its very low absorption intensity. We demonstrate how a low pressure of 3.3 GPa strongly increases the strength of the electromagnon and expands its existence to a large temperature range enhanced by 40 K. Accordingly, these two combined effects make the electromagnon of CuO under pressure a more ductile quantum object. Numerical simulations based on an extended Heisenberg model were combined to the Monte-Carlo technique and spin dynamics to account for the magnetic phase diagram of CuO. They enable to simulate the absorbance response of the CuO electromagnons in the THz range

    Cytological and histological detection of amyloid deposits in bone marrow of patients affected by multiple myeloma.

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    We recently published a study aiming to verify the frequency of amyloid deposits in the bone marrow of patients with multiple myeloma (MM) who did not present any signs or symptoms of systemic amyloidosis, applying the Congo red technique on bone marrow smears obtained by aspiration from the posterior iliac spine. The results suggested that nearly 40% of patients affected by MM may have amyloid deposits in their bone marrow. Subsequently, this finding has not been confirmed by another study performed with histological specimens of bone marrow in a similar clinical setting. To explain this discrepancy, we performed a comparative study on the bone marrows of 36 patients affected by MM, evaluated by both cytological and histological techniques. The results of this study confirm the high frequency of amyloid deposits in the bone marrow of patients affected by MM when the analysis is made on cytological smears, and indicate that the presence of amyloid on marrow smears is confirmed by core biopsies simultaneously performed in only 25% of cases. Should further studies confirm our findings, cytological assessment could be considered a sensitive technique to detect bone marrow amyloid deposits
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