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Liver abscess and endogenous endophthalmitis secondary to Klebsiella variicola in a patient with diabetes: first reported case.

Authors:
Saúl Villoria Díaz Jesús Alberto Piñuel González Alicia Galindo-Ferreiro Paola Stefanía Calles Monar Ana María Alonso Tarancón Marina Pilar González de Frutos

Arq Bras Oftalmol 2022 May-Jun;85(3):324-326

Department of Ophthalmology, Complejo Asistencial Universitario de Palencia, Palencia, Spain.

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http://dx.doi.org/10.5935/0004-2749.202200104DOI Listing
June 2022

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Histiocytic Sarcoma With CCND1 Gene Rearrangement Clonally Related and Transdifferentiated From Mantle Cell Lymphoma.

Authors:
Jyoti Kumar Mustafa Al-Kawaaz Brock A Martin Mohamed M Hegazi Brent Tan Dita Gratzinger

Am J Clin Pathol 2022 Aug 14. Epub 2022 Aug 14.

Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.

Objectives: Histiocytic neoplasms demonstrate shared gene translocations and clonal immunoglobulin gene rearrangements in cases of associated B-cell lymphomas. However, the evolution of these related disease processes remains largely uncertain, especially in the setting of a prior mantle cell lymphoma.

Methods: We describe a unique case of a histiocytic sarcoma that transdifferentiated from blastoid mantle cell lymphoma after extensive therapy. Read More

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August 2022
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Short stature and melanocytic nevi in a girl with ARID1B-related Coffin-Siris syndrome: a case report.

Authors:
Dong-Ying Tao Huan-Hong Niu Jing-Jing Zhang Hui-Qin Zhang Ming-Hua Zeng Sheng-Quan Cheng

BMC Pediatr 2022 Aug 13;22(1):486. Epub 2022 Aug 13.

Department of Pediatrics, Xijing Hospital, Fourth Military Medical University, No. 127 Changle West Road, Xincheng District, Xi'an, 710032, Shaanxi Province, China.

Background: Coffin-Siris syndrome (CSS) is a rare autosomal dominant disorder characterized by intellectual disability, developmental delay, and characteristic facial features. Few patients with cutaneous phenotype in this rare syndrome have been reported.

Case Presentation: Herein, we describe a 12-year-old Chinese girl diagnosed with CSS, who was referred to our hospital because of intellectual disability and short stature. Read More

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Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis.

Authors:
Gregorio Serra Luigi Memo Paola Cavicchioli Mario Cutrone Mario Giuffrè Maria Laura La Torre Ingrid Anne Mandy Schierz Giovanni Corsello

Ital J Pediatr 2022 Aug 13;48(1):145. Epub 2022 Aug 13.

Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties "G. D'Alessandro", University of Palermo, Palermo, Italy.

Background: Congenital ichthyosis (CI) is a heterogeneous group of genetic disorders characterized by generalized dry skin, scaling and hyperkeratosis, often associated to erythroderma. They are rare diseases, with overall incidence of 6.7 in 100,000. Read More

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Serum proteomics of severe fever with thrombocytopenia syndrome patients.

Authors:
Sang-Yeop Lee Sung Ho Yun Hayoung Lee Yun Gyeong Lee Giwan Seo Nam Hoon Kim Edmond Changkyun Park Chang-Seop Lee Seung Il Kim

Clin Proteomics 2022 Aug 13;19(1):32. Epub 2022 Aug 13.

Research Center for Bioconvergence Analysis, Korea Basic Science Institute, Ochang, 28119, Republic of Korea.

Background: Dabie bandavirus, also termed as severe fever with thrombocytopenia syndrome virus (SFTSV), was first isolated in China in 2010. At this time, the virus was found to have spread to South Korea, Japan, and other countries. A high case fatality rate is reported for SFTS, ranging from 12-50% within various sources. Read More

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Authors:
Alexandru Achim Stefan Harb Gabor G Toth Lian Krivoshei Gregor Leibundgut

Cardiovasc Revasc Med 2022 Aug 8. Epub 2022 Aug 8.

Klinik für Kardiologie, Medizinische Universitätsklinik, Kantonsspital Baselland, Liestal, Switzerland. Electronic address:

Coronary perforation leading to shunting to other cardiac chambers is a rare complication of percutaneous coronary intervention (PCI), and most cases reported aggressive treatment with either a covered stent, coiling, or protamine injection. We report herein two cases, one of a fairly large cavity-spilling perforation of the left anterior descending coronary artery into the right ventricle and one spilling in the coronary vein. Both iatrogenic shunts were treated conservatively, and angiographic follow-up showed spontaneous resolution, suggesting that the outcome in this type of perforation may be favorable with conservative therapy. Read More

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August 2022
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