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New perspectives on documenting Attic pottery, in Baldoni V. (ed.), From Pottery to Context. Archaeology and Virtual Modelling
The study of the Attic-figured pottery is closely connected with the Beazley methods, which consists in the possibility of recognizing a painting hand exclusively based on the style of the work; the Beazley method, despite having suffered some criticism, is still considered substantially valid. The need to have images which can be analyzed from a stylistic point of view, has suggested to combine the use of some open-source programs of 3D photogrammetry (such as VisualSFM and Meshlab) and 3D modeling (such as Blender), in order to shift the figured frieze from the pot to paper, avoiding the limitations associated with traditional direct drawing
Antefixes from Museo Provinciale Campano in Capua. A proposal for a virtual reconstruction, in Baldoni V. (ed.), From Pottery to Context. Archaeology and Virtual Modelling
The paper aims to illustrate an intervention of digital restoration carried out on different groups of antefixes coming from excavations started in 1845 in a private fund today located in Curti, near Caserta and pertaining to sacred building roofs of a sanctuary whose oldest phase is dated to the 6th century BC. Nowadays, finds are preserved in the Museo Provinciale Campano, located in Capua. Particularly, two hundred and fifty antefixes belonging to the group named â female heads within the nimbus, have been studied, articulated into thirty different series, filed in a database created ad hoc, and the digital restoration of their prototypes has been completed. Issues relating to seriality and traceability of these finds to individual archetypes will be explored, features that make a faithful 3D reconstruction of a prototype possible, based on the combination of physical data of fragmented antefixes pertaining to each series. Furthermore, phases and techniques of detection and scanning of an archaeological find using a laser scanner for small objects will be particularly analyzed. It will show how to achieve a mesh from a scanning file and how to elaborate it. Lastly, processing steps necessary to the realization of a 3D restoration will be illustrated through modeling techniques and collation of different 3D scannings. These kinds of technological experimentations contribute to diversify our memory transmission modes. They offer the chance to create digital and implementable catalogs, useful for a dynamic documentation of the Archaeological Heritage, but also and above all, fundamental tools for the monitoring, conservation and fruition of analyzed corpora
Cryptogenic Fibrosing Pleuritis
We report the case of a 46-year-old male patient who was referred for chest pain and bilateral pleural effusion. Despite treatment with antibiotics and steroids, the pleural effusion worsened over a few months until pulmonary function was halved. The CT scan showed bilateral pleural thickening with right basal opacity. Histology revealed extensive fibrotic tissue with focal collections of lymphocytes and giant cells without traces of asbestos bodies. Since no evidence of an infectious, embolic or occupational aetiology was found, this bilateral pleural effusion progressing to diffuse pleural thickening was diagnosed as cryptogenic fibrosing pleuritis, a rare pleural disease
Difficult to Diagnose the Cause of Intestinal Obstruction due to Abdominal Cocoon Syndrome
Abdominal cocoon syndrome (sclerosing encapsulating peritonitis) is a rare condition associated with clinical signs of intestinal dysfunction, episodes of small bowel obstruction and sometimes a palpable abdominal mass. We present the case of a 46-year-old male patient with
clinical signs of intestinal obstruction caused by primary sclerosing encapsulating peritonitis
Hashimoto's Thyroiditis-Associated Acute Renal Failure and Pitfalls of eGFR Interpretation in Thyroid Diseases
The authors describe a patient with severe hypothyroidism due to Hashimoto’s thyroiditis and describe the pitfalls of estimated glomerular filtration rate interpretation in such cases
Unusual Fatal Outcome Following Administration of a Combination of anti-PD1 and anti-CTLA4 in Metastatic Renal Cell Carcinoma: Liver Toxicity Case Report and a Literature Review
Hepatic dysfunction, in the absence of liver metastases, occurs in 10–15% of renal cell carcinoma (RCC) patients, while immune hepatitis due to anti-CTLA4 and anti-PD1 administration affects about 3–9% and 0.7–1.8% of treated patients, respectively. Liver toxicity following
combination therapy (anti-CTLA4 and anti-PD1) is seen in 29% of patients overall and grade 3–4 toxicity in 14% of patients.Stauffer’s syndrome is a rare para-neoplastic phenomenon associated with RCC and characterized by abnormal liver function tests, hepato-splenomegaly and histological changes consistent with non-specific hepatitis. We describe a case of RCC treated with anti-CTLA4 and anti-PD1 therapy resulting in immediate liver toxicity and death after 2 months of progressive hepatic impairment. We hypothesize that high IL-6 levels due to Stauffer’s syndrome might have contributed to immune-related hepatic failure
Kluver-Bucy Syndrome: A Rare Complication of Herpes Simplex Encephalitis
Kluver-Bucy syndrome (KBS) is a characterized by a group of cognitive dysfunctions that include hypersexuality, placidity, hyperorality, memory deficits and hypermetamorphosis. This syndrome is often seen in pathological states that destroy the temporal lobes, normally bilaterally. Herpes simplex encephalitis (HSE) is one of the causes of KBS, as the herpes virus can cause dysfunction/destruction of the temporal lobes. KBS is a very rare syndrome, with just a few cases described in the literature. We present the case of a 21-year-old-man who was diagnosis with KBS after HSE
A Case of Ticagrelor Resistance
Ticagrelor is a directly acting cyclopentyltriazolo-pyrimidine which does not require conversion into an active metabolite. It inhibits the P2Y12 receptors on platelets reversibly. Unlike clopidogrel and prasugrel, resistance to ticagrelor is rarely reported. Various mechanisms have been proposed for this resistance. The case of a 62-year-old man with diabetes who had undergone index percutaneous coronary intervention (PCI) 22 days previously is described. The patient presented to us with stent thrombosis. His primary PCI was successfully carried out with a drug-eluting stent. He showed resistance to ticagrelor on thromboelastography platelet mapping. He responded well to prasugrel (another P2Y12 inhibitor) in combination with aspirin
Pulmonary Embolism in Autosomal Dominant Polycystic Kidney Patient Induced by Inferior Vena Cava Mechanical Compression
Introduction: Autosomal dominant polycystic kidney disease is a common syndrome. Renal and hepatic cysts can cause discomfort, bleeding, rupture, infection, hypertension and a mass effect with compression of adjacent organs.Case presentation: A 48-year-old man with polycystic kidney disease and hypertension presented to the emergency department for bilateral flank pain. An abdominal computed tomography scan with contrast showed a 7 cm heterogeneous process posteriorly and laterally to the right kidney. It appeared to be a renal cyst associated with bleeding and bilateral pulmonary artery filling defects, apparently due to pulmonary embolism. Cavography following inferior vena cava filter insertion did not show any deep vein thrombosis. Discussion and conclusion: The pulmonary embolism was probably caused by extrinsic inferior vena cava compression by a liver cyst. Virchow's triad of stasis, vessel damage and hypercoagulability probably resulted in a thrombus which moved on the right side to the pulmonary artery