Campiglia Marittima Skarn (Tuscany): A Challenging Example for the Evolution of Skarn-Forming Models

Campiglia Marittima (hereafter Campiglia) has a long record of attracting interest on its ore deposits that have been intermittently exploited from the Copper Age to the late XX century. Since the XIX century, Campiglia has been a key locality for the debate on skarn-forming processes due to the presence of mining activities ensuring access to ever new rock exposures. The pioneering study of vom Rath and the comparison with attractive chemical model (e.g., Korzhinskii's theory) in the XX century made Campiglia a "classic" example of skarn ore deposit, from the causative intrusion to the marble host rock. In recent years, detailed field investigations integrated by petrographic, geochemical, and isotopic analyses revealed a more complex and stimulating geological history. The Campiglia skarn was later intruded by mafic magma causing textural reworking and chemical redistribution as well as the reverse telescoping process with Fe-Cu sulfides overprinting previously formed Pb-Zn ore. This work aims to trace the evolution of the scientific thinking on the Campiglia ore deposit by comparison with existing skarn-forming models and, ultimately, shows that the current skarn-forming model(s) cannot fully explain the textural and geochemical features of the Campiglia skarn

Prevalence of Primary Radiographic Signs of Hip Dysplasia in Dogs

Hip dysplasia is a disabling orthopedic disease in dogs. The aim of this retrospective study was to evaluate the morphological aspects and radiographic changes in the development of hip dysplasia in adult dogs, and to describe the frequency of each radiographic parameter according to each Federation Cynologique Internationale (FCI) grade. Brass descriptive forms for the evaluation of hip dysplasia were obtained from the archive of the Italian Fondazione Salute Animale, and the radiographic evaluation of 642 hips were processed. Sixteen radiographic criteria were assessed, divided into six main parameters: acetabulum, femoral head and its position in the acetabulum, femoral neck, joint space, and Norberg angle. The initial mild alterations were shown in the craniolateral acetabular rim (31.8%), slightly divergent in the joint space in 58.6% of FCI-A. The spherical shape of the femoral head was mildly small/flattened in 56.9% of FCI-B, in addition to a slightly cylindrical-shaped femoral neck (60.5%) and slightly lost contours (55.0%). Changes in acetabular depth (45.0%), and in the cranial acetabular margin (56.7%) were found in FCI-C. The center of the femoral head was lateral to the dorsal acetabular rim in 70.0% of FCI-B; the Norberg angle appeared normal in 70.6% of FCI-B. Elaboration of the radiographic criteria from the Brass descriptive forms allowed for the extrapolation of accurate knowledge regarding morphologic changes in the development of dysplasia by providing detailed information for each individual. In particular, the present survey showed that the morphological alterations of the acetabulum prevailed over those of the femoral head only at the beginning of the development of canine hip dysplasia, and then worsened after the changes occurred in the femoral head and neck

Characterization of FCI (Fédération Cynologique Internationale) Grades for Hip Dysplasia in Five Dog Breeds

Simple Summary Hip dysplasia is one of the most frequently occurring orthopedic diseases in medium to large purebred dogs. For this reason, much attention is paid to screening programs for breeding animals. The Federation Cynologique Internationale uses the same evaluation criteria regardless of breed. The aim of this study was to evaluate whether or not the evolution of a hip pathology in dogs with or without dysplasia was consistent with prior scientific knowledge in five breeds. In addition, whether there were significant radiographic differences between breeds which might require a breed-specific method for assessing the grade of hip dysplasia was investigated. Evaluations of 16 radiographic parameters analyzed using the Brass method were collected from 5 breeds: Labrador Retrievers, Golden Retrievers, German Shepherd dogs, Bernese Mountain dogs, and Rottweilers. No significant changes were found among the five breeds regarding the grade of hip dysplasia; however, some significant variations were found in the individual radiographic parameters suggesting that, although the criteria regarded all breeds, there were specific alterations which could be caused by the different morphologies, aptitudes and abilities of each breed. The aim of this retrospective study was to verify whether the radiographic morphologic differences detected within the first three grades of hip dysplasia (A, B, C) of each of the five selected breeds and within the same breeds were statistically significant enough to require a breed-specific evaluation. A total of 422 technical evaluation forms of hip dysplasia (HD) in Labrador Retrievers, Golden Retrievers, Rottweilers, Bernese Mountain dogs, and German Shepherd dogs were obtained from the Federation Cynologique Internationale (FCI) archive. The data were evaluated using a descriptive statistical analysis. In Labrador Retrievers, the craniolateral acetabular rim and femoral head position were already altered in unaffected dogs; however, within the various FCI grades, the most severe changes involved the conformation of the femoral neck. All the radiographic parameters of the Golden Retriever hips changed progressively and evenly. Significant radiographic changes between FCI grades were found in the German Shepherd dogs, and the alterations involving the acetabulum were more severe and appeared earlier than in the femoral head and neck. In the Bernese Mountain dogs, the most severe alterations were in the position of the femoral head and joint space while the femoral head and neck showed no significant progression between grades. All the radiographic parameters of non-dysplastic Rottweilers were normal; however, the progression of the primary signs was similar to the other breeds, although with lower severity. In conclusion, no significant prevalence of the radiographic features was observed for any specific breed. However, significant individual breed variations in the primary radiographic parameters were found between dogs with and without dysplasia which could be useful for better understanding the consequences of biomechanical differences between breeds

Time-space focused intrusion of genetically unrelated arc magmas in the early Paleozoic Ross-Delamerian Orogen (Morozumi Range, Antarctica)

The growth of continental crust in accretionary orogenic belts takes place through repeated cycles of subduction– accretion of rock units fromcontinental and oceanic magmatic arcs, supra-subduction zone backarcs and forearcs loaded with continent-derived materials. An ancient example relevant to magmatic arc accretion models is represented by the remnants of the Cambrian–Ordovician Ross Orogen in the Morozumi Range, Victoria Land (Antarctica). There, late Neoproterozoic phyllites host an intrusive complex which preserves a remarkably uncommon record of genetically unrelated magma pulses emplaced under a variable stress regime in a short time span: (1) a dominant K-feldspar–phyric granite, (2) fine-grained dioritic stocks and dykes, (3) a peraluminous granite; and (4) a tonalitic–granodioritic dyke swarm. Laserprobe U–Pb zircon dates cluster at late Cambrian times for all these units, yet they carry differential cargoes of relict cores. Unique geochemical– isotopic signatures for both the less evolved magmas (diorite and dyke tonalite) and the most acidic ones (granite and peraluminous granite) indicate that each one of them originated from distinct sources at depth. Additionally, field relationships and chemical evolutionary trends testify for a variety of shallow level open-system processes, such as magma mingling/mixing between diorite and main granite magmas, as well as progressive incorporation of the host schists by the dyke tonalite magma. In summary, crustal growth in the Morozumi intrusive complex was contributed by fresh mantle magma issuing from the metasomatised mantle wedge, while the production of othermelts did recycle different crustal portions/layers: the main granite derived fromGrenville-age granulitic lower crust; the peraluminous granite from late Proterozoic upper crust, and the tonalite magmas derived from subduction erosion-enriched subarc mantle and evolved by ingestion of local metasedimentary rocks. Overall, the Morozumi intrusive complex yields evidence for emplacement in the same site at the same time of magmas issuing fromdifferent sources that are usually found at a different depth in the arc lithospheric section. A likely scenario to activate this specific mechanism of melt production is a subduction zone affected by subduction erosion

Creencias de los profesionales de salud mental en la clínica de las adicciones y el impacto en la efectividad de los tratamientos

El presente trabajo tiene como objetivo comprender las creencias de los profesionales de salud mental que trabajan en la clínica de las adicciones en centros públicos de tratamientos y el impacto de las mismas en la efectividad de los tratamientos en los Centros Preventivos Asistenciales en Adicciones (CPAA) Públicos de la provincia de Mendoza. Pues dichas creencias condicionan la forma de entender las distintas disciplinas y las formas de practicarlas y orientar y guiar las intervenciones en la clínica de las adicciones

A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient

Human malignant autosomal recessive osteopetrosis (ARO) is a genetically heterogeneous disorder caused by reduced bone resorption by osteoclasts. Mutations in the CLCN7 gene are responsible not only for a substantial portion of ARO patients, but also for other forms of osteopetrosis characterized by different severity and inheritance. The lack of a clear genotype/phenotype correlation makes genetic counselling a tricky issue for CLCN7-dependent osteopetrosis. Here we characterize the first homozygous interstitial deletion in 16p13.3, detected by array Comparative Genomic Hybridization (a-CGH) in an ARO patient of Jordanian origin. The deletion involved other genes beside CLCN7, while the proband displayed a classic ARO phenotype; however her early death did not allow more extensive clinical investigations. The identification of this novel genomic deletion involving a large part of the CLCN7 gene is of clinical relevance, especially in prenatal diagnosis, and suggests the possibility that this kind of mutation has been underestimated so far. This data highlights the need for alternative approaches to genetic analysis also in other ARO-causative genes

Hypomorphic mutation in the RAG2 gene affects dendritic cell distribution and migration.

In Omenn syndrome, altered dendritic cell distribution and impaired migration represent an additional level of immune dysregulation, contributing to the pathogenesis of autoimmunity. OS is a severe combined immunodeficiency characterized by erythrodermia and protracted diarrhea as a result of infiltration of oligoclonal-activated T cells, caused by hypomorphic mutations in RAGs. The RAG2(R229Q) mouse model fully recapitulates the clinical OS phenotype. We evaluated whether T and B cell defects, together with the abnormal lymphoid structure, could affect DC homeostasis and function. High density of LCs was observed in skin biopsies of Omenn patients and in the derma of RAG2(R229Q) mice, correlating with the presence of erythrodermia. In vivo models of cutaneous skin painting and CHS demonstrated a decreased migration of RAG2(R229Q) DCsin particular, LCsinto draining LNs. Interestingly, at steady state, RAG2(R229Q) mice showed a reduction in DC number in all hematopoietic organs except LNs. Analysis of the MHCII marker revealed a diminished expression also upon the LPS-driven inflammatory condition. Despite the decreased number of peripheral DCs, BM pre-cDCs were present in normal number compared with RAG2(+/+) controls, whereas pDCs and monocytes were reduced significantly. Overall, these results point to a secondary defect in the DC compartment, which contributes to clinical manifestations and autoimmunity in OS

Adherent Serous Crust of the Scalp: Inflammatory or Infectious Hair Disease? A Case of Scalp Eschar and Neck Lymph Adenopathy after a Tick Bite

Scalp eschar and neck lymphadenopathy after tick bite (SENLAT) is an emerging and increasingly common syndrome, primarily described in Europe..

Inverse psoriasis in patient treated with atezolizumab

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Dendritic Cells Cause Bone Lesions in a New Mouse Model of Histiocytosis.

Langerhans cell histiocytosis (LCH) is a rare disease caused by the clonal accumulation of dendritic Langerhans cells, which is often accompanied by osteolytic lesions. It has been reported that osteoclast-like cells play a major role in the pathogenic bone destruction seen in patients with LCH and these cells are postulated to originate from the fusion of DCs. However, due to the lack of reliable animal models the pathogenesis of LCH is still poorly understood. In this study, we have established a mouse model of histiocytosis- recapitulating human disease for osteolytic lesions seen in LCH patients. At 12 weeks after birth, severe bone lesions were observed in our multisystem histiocytosis (Mushi) model, when CD8α conventional dendritic cells (DCs) are transformed (MuTuDC) and accumulate. Most importantly, our study demonstrates that bone loss in LCH can be accounted for the transdifferentiation of MuTuDCs into functional osteoclasts both in vivo and in vitro. Moreover, we have shown that injected MuTuDCs reverse the osteopetrotic phenotype of oc/oc mice in vivo. In conclusion, our results support a crucial role of DCs in bone lesions in histiocytosis patients. Furthermore, our new model of LCH based on adoptive transfer of MuTuDC lines, leading to bone lesions within 1-2 weeks, will be an important tool for investigating the pathophysiology of this disease and ultimately for evaluating the potential of anti-resorptive drugs for the treatment of bone lesions