20 research outputs found

    Breast Cancer with Cartilaginous and/or Osseous Metaplasia Diagnosed by Lymph Nodal Metastasis:A Case Report

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    Breast cancer with cartilaginous and/or osseous metaplasia is a type of metaplastic carcinomas and is a rare disease. We report the case of a 49 year-old female who underwent right mastectomy for a large breast tumor. Histological examinations revealed a mixed tumor with both stromal and epithelial elements;the stroma showed poor differentiated spindle-shape and multiform cells with a massive osseous matrix, and atypical epithelial cells, which mainly existed on the surface of the cysts, showed nucleic atypia. The tumor was diagnosed as a malignant phyllodes tumor with osteosarcomatous differentiation;it was not identified as a metaplastic carcinoma because of the lack of proof of a cancerous component. Two years after a mastectomy, swelling of the axillary lymph nodes was found and a biopsy was performed. Histological findings for the lymph node indicated a metastasis of the invasive ductal carcinoma. The primary tumor was re-examined and was considered to be the origin of the lymph nodal metastasis. Lymph nodal metastasis of cancer proved that the primary tumor had cancerous potential, and the pathological diagnosis was altered to a breast cancer with cartilaginous and/or osseous metaplasia.</p

    Abscess Formation of the Round Ligament of the Liver: Report of a Case

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    Abscess formation of the round ligament of the liver is very rare. We report a case of a 70-year-old female with abscess of the round ligament after an endoscopic papillotomy for choledocholithiasis. On the 21st day following papillotomy, abscess formation of the round ligament was found by ultrasonographic examination. Surgical treatment was performed because conservative therapy was not effective. The purulent fluid and necrotic tissue at the round ligament were completely removed. Cultures obtained from the abscess grew Staphylococcus epidermidis, but the mechanism of abscess formation in this case remains unclear.</p

    Unusual Redox Behavior of Rh/AlPO<sub>4</sub> and Its Impact on Three-Way Catalysis

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    The influence of the redox behavior of Rh/AlPO<sub>4</sub> on automotive three-way catalysis (TWC) was studied to correlate catalytic activity with thermal stability and metal–support interactions. Compared with a reference Rh/Al<sub>2</sub>O<sub>3</sub> catalyst, Rh/AlPO<sub>4</sub> exhibited a much higher stability against thermal aging under an oxidizing atmosphere; further deactivation was induced by a high-temperature reduction treatment. In situ X-ray absorption fine structure experiments revealed a higher reducibility of Rh oxide (RhO<sub><i>x</i></sub>) to Rh, and the metal showed a higher tolerance to reoxidation when supported on AlPO<sub>4</sub> compared with Al<sub>2</sub>O<sub>3</sub>. This unusual redox behavior is associated with an Rh–O–P interfacial linkage, which is preserved under oxidizing and reducing atmospheres. Another effect of the Rh–O–P interfacial linkage was observed for the metallic Rh with an electron-deficient character. This leads to the decreasing back-donation from Rh <i>d</i>-orbitals to the antibonding π* orbital of chemisorbed CO or NO, which is a possible reason for the deactivation by high-temperature reduction treatments. On the other hand, surface acid sites on AlPO<sub>4</sub> promoted oxidative adsorption of C<sub>3</sub>H<sub>6</sub> as aldehyde, which showed a higher reactivity toward O<sub>2</sub>, as well as NO, compared with carboxylate adsorbed on Al<sub>2</sub>O<sub>3</sub>. A precise control of the acid–base character of the metal phosphate supports is therefore a key to enhance the catalytic performance of supported Rh catalysts for TWC applications

    Rhodium Nanoparticle Anchoring on AlPO<sub>4</sub> for Efficient Catalyst Sintering Suppression

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    Rhodium catalysts exhibited higher dispersion with tridymite-type AlPO<sub>4</sub> supports than with Al<sub>2</sub>O<sub>3</sub> during thermal aging at 900 °C under an oxidizing atmosphere. The local structural analysis via X-ray photoelectron spectroscopy, transmission electron microscopy, X-ray absorption fine structure, and infrared spectroscopy suggested that the sintering of AlPO<sub>4</sub>-supported Rh nanoparticles was significantly suppressed because of anchoring via a Rh–O–P linkage at the interface between the metal and support. Most of the AlPO<sub>4</sub> surface was terminated by phosphate P–OH groups, which were converted into a Rh–O–P linkage when Rh oxide (RhO<sub><i>x</i></sub>) was loaded. This interaction enables the thin planar RhO<sub><i>x</i></sub> nanoparticles to establish close and stable contact with the AlPO<sub>4</sub> surface. It differs from Rh–O–Al bonding in the oxide-supported catalyst Rh/Al<sub>2</sub>O<sub>3</sub>, which causes undesired solid reactions that yield deactivated phases. The Rh–O–P interfacial linkage was preserved under oxidizing and reducing atmospheres, which contrasts with conventional metal oxide supports that only present the anchoring effect under an oxidizing atmosphere. These experimental results agree with a density functional theory optimized coherent interface RhO<sub><i>x</i></sub>/AlPO<sub>4</sub> model

    Tuning the Electron Density of Rh Supported on Metal Phosphates for Three-Way Catalysis

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    The automotive three-way catalysis (TWC) performance of Rh supported on alkaline-earth and rare-earth phosphates was studied in comparison to that of Rh on aluminum phosphate (AlPO<sub>4</sub>). The anchoring of Rh via interfacial Rh–O–P bonding in Rh/AlPO<sub>4</sub> leads to efficient Rh sintering suppression. However, the electron-withdrawing nature of the phosphate affords electron-deficient Rh, which has a negative impact on its catalytic activity under a reducing atmosphere due to a decrease in back-donation from the Rh <i>d</i>-orbitals to the antibonding π* orbitals of adsorbed CO and NO molecules. Notably, the extent of this electron deficiency could successfully be reduced by replacing AlPO<sub>4</sub> with alkaline-earth or rare-earth phosphates, and the Rh oxide formed on these phosphate supports was readily reduced to metallic Rh. This behavior is in complete contrast to that of corresponding metal oxide supports, because the higher basicity of these supports yields Rh oxides that are more difficult to reduce. Among the phosphate-supported catalysts investigated in the present study, Rh/LaPO<sub>4</sub> demonstrated the highest TWC performance after thermal aging under both oxidizing and reducing atmospheres. The effect of the higher basicity of LaPO<sub>4</sub> compared to that of AlPO<sub>4</sub> is most obvious in its improved catalytic activity for elementary CO–O<sub>2</sub>, CO–H<sub>2</sub>O, and CO–NO reactions. Importantly, this improvement is achieved while maintaining the activity toward C<sub>3</sub>H<sub>6</sub> as an advanced feature of phosphate supports

    Rh/ZrP<sub>2</sub>O<sub>7</sub> as an Efficient Automotive Catalyst for NO<sub><i>x</i></sub> Reduction under Slightly Lean Conditions

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    The three-way catalyst performances of honeycomb-coated Rh catalysts were studied on several metal phosphate supports (AlPO<sub>4</sub>, YPO<sub>4</sub>, ZrP<sub>2</sub>O<sub>7</sub>, and LaPO<sub>4</sub>) using various simulated exhausts with different air-to-fuel ratios (<i>A</i>/<i>F</i>). These supports significantly improved the NO<sub><i>x</i></sub> purification (deNO<sub><i>x</i></sub>) efficiency under slightly lean conditions (14.6 < <i>A</i>/<i>F</i> ≤ 15.3) as compared with conventional Rh/ZrO<sub>2</sub> catalysts. The deNO<sub><i>x</i></sub> activity exhibited the following sequence of increasing the mean electronegativity of the supports: ZrO<sub>2</sub> < YPO<sub>4</sub> < LaPO<sub>4</sub> < AlPO<sub>4</sub> < ZrP<sub>2</sub>O<sub>7</sub>. Although both NO–CO and NO–C<sub>3</sub>H<sub>6</sub> reactions contributed to the deNO<sub><i>x</i></sub> process, the latter reaction was more favored on Rh/ZrP<sub>2</sub>O<sub>7</sub> than on Rh/ZrO<sub>2</sub>. Partially oxidized C<sub>3</sub>H<sub>6</sub> was adsorbed on Rh/ZrP<sub>2</sub>O<sub>7</sub> in the form of reactive aldehyde species, in contrast to the less-reactive carboxylate species adsorbed on Rh/ZrO<sub>2</sub>. Furthermore, Rh oxide was more easily reduced to the active metallic state on ZrP<sub>2</sub>O<sub>7</sub> compared with Rh/ZrO<sub>2</sub> when the atmosphere was changed from lean (<i>A</i>/<i>F</i> > 14.6) to rich (<i>A</i>/<i>F</i> < 14.6). Metallic Rh formed on ZrP<sub>2</sub>O<sub>7</sub> was only slowly oxidized on exposure to excess O<sub>2</sub>, whereas Rh on ZrO<sub>2</sub> was readily oxidized to less-active Rh<sub>2</sub>O<sub>3</sub>. The high activity of Rh/ZrP<sub>2</sub>O<sub>7</sub> toward C<sub>3</sub>H<sub>6</sub> oxidation via aldehyde species as well as the resistance of metallic Rh against reoxidation are considered to be possible reasons for the enhanced deNO<sub><i>x</i></sub> performance of this catalyst in a slightly lean region

    Fibrous hamartoma of infancy in the scrotum – Report of a case

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    Fibrous hamartomas of infancy (FHI) is rare benign tumors. FHI is typically present before the age of two years. We report a 13-month-old child with FHI, which presented as the growing scrotum mass clinically diagnosed rhabdomyosarcoma of the trunk. Right scrotal swelling was presented. The mass was irregular, solidly, and non-tender. Operative findings revealed a mass fixed to the scrotal fundus. FHI is differentiated from other malignant neoplasms in the scrotum
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