Case reports in clinical pathology最新文献_第4页

A peculiar uncommon cutaneous neoplasia: Angiosarcoma of the head and neck of the elderly (Wilson Jones Angiosarcoma) 一种罕见的皮肤肿瘤:老年人头颈部血管肉瘤(威尔逊·琼斯血管肉瘤)

Case reports in clinical pathology Pub Date : 2019-07-19 DOI: 10.5430/CRCP.V6N1P9

A. D'Amuri, Federica Floccari, R. Filotico, M. Filotico

引用次数: 0

Eosinophilic peritonitis in a patient with liver cirrhosis: A case report 肝硬化患者嗜酸性腹膜炎1例

Case reports in clinical pathology Pub Date : 2019-06-04 DOI: 10.5430/CRCP.V6N1P5

M-H Pang, F. Hua, Yixiao Zhi, E. Qin, Y. Tao, Rui Hua

{"title":"Eosinophilic peritonitis in a patient with liver cirrhosis: A case report","authors":"M-H Pang, F. Hua, Yixiao Zhi, E. Qin, Y. Tao, Rui Hua","doi":"10.5430/CRCP.V6N1P5","DOIUrl":"https://doi.org/10.5430/CRCP.V6N1P5","url":null,"abstract":"Eosinophilic gastroenteritis (EG) is a gastrointestinal disease characterized by abnormal infiltration of eosinophilic cells in the gastrointestinal tract, excluding known causes of eosinophilia. Eosinophilic peritonitis (EP) is rare and is considered by most scholars to be a systemic or local allergy to exogenous or endogenous allergens. It is a clinical manifestation of eosinophilic gastroenteritis involving the serosal layer. Hereby, we report a case of EP in a patient with liver cirrhosis. A 32-year-old man was admitted to our hospital for intermittent fatigue, abdominal distension and abdominal pain. On account of clinical feature and pathological results of peritoneal puncture biopsy, excluding other causes of peripheral eosinophilia, the diagnosis of EP with hepatic cirrhosis was established. The possibility of EP should be paid great attention to patients with cirrhosis with peritonitis. Gastrointestinal endoscope biopsy, laparoscopy or peritoneal puncture biopsy are conducive to the diagnosis and differential diagnosis. Therefore, once the disease is suspected, gastrointestinal endoscope biopsy should be performed actively, and multiple pathological samples should be taken to contribute to diagnosis and treatment. Laparoscopy or peritoneal puncture biopsy is of vital significance for definitive diagnosis. ","PeriodicalId":90463,"journal":{"name":"Case reports in clinical pathology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.5430/CRCP.V6N1P5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48454651","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Acute transaminitis as an atypical presentation of Graft-versus-Host Disease following Hematopoietic Stem Cell Transplantation 急性转氨炎是造血干细胞移植后移植物抗宿主病的不典型表现

Case reports in clinical pathology Pub Date : 2019-03-25 DOI: 10.5430/CRCP.V6N1P1

R. Ramkissoon, A. Shetty, Adam C Doyle, O. Adeyi, K. Patel

引用次数: 0

Clear cell renal cell carcinoma with heterotopic bone formation: A case report and literature review 透明细胞肾细胞癌伴异位成骨1例并文献复习

Case reports in clinical pathology Pub Date : 2019-01-15 DOI: 10.5430/CRCP.V5N2P16

Estelle Oertling, Cacey Peters, R. Wood, J. Silberstein, Andrew B. Sholl, Nadja K. Falk

引用次数: 0

Angiolymphoid hyperplasia with eosinophilia: An uncommon presentation and novel treatment of a rare disease 血管淋巴样增生伴嗜酸性粒细胞增多：一种罕见疾病的罕见表现和新的治疗方法

Case reports in clinical pathology Pub Date : 2018-12-30 DOI: 10.5430/CRCP.V5N2P12

D. Surprenant, Amanda Goslawski, Karen C Kagha, D. Griffin, K. Mudaliar, K. Hutchens, D. Opel, R. Tung

引用次数: 1

SDHB mutated paraganglioma imitating thyroid tumor: A case report and review of literature SDHB突变的模仿甲状腺肿瘤的副神经节瘤1例报告及文献复习

Case reports in clinical pathology Pub Date : 2018-08-28 DOI: 10.5430/CRCP.V5N2P5

Vygantė Maskoliūnaitė, G. Makunaite, A. Garnelytė, A. Abraitienė, V. Beisa

{"title":"SDHB mutated paraganglioma imitating thyroid tumor: A case report and review of literature","authors":"Vygantė Maskoliūnaitė, G. Makunaite, A. Garnelytė, A. Abraitienė, V. Beisa","doi":"10.5430/CRCP.V5N2P5","DOIUrl":"https://doi.org/10.5430/CRCP.V5N2P5","url":null,"abstract":"Paragangliomas of the head and neck are uncommon tumors arising from parasympathetic ganglia. Paragangliomas are mostly asymptomatic and may manifest as palpable mass of neck. The morphologic features are non-specific and comparable to the other neuroendocrine tumors. Most of hereditary cases are associated with alterations in genes of succinate dehydrogenase (SDH). SDHA and SDHB immunohistochemistry is considered as reliable screening method to detect tumors with genetical alterations. Of note, SDHB mutated paragangliomas have the highest risk of local recurrence, distant metastasis and the development of other tumor phenotypes, which are associated with mutation. Therefore, active surveillance of patients and early surgical treatment are essential. In contrast, SDHB mutated head and neck paragangliomas was considered as completely benign tumors, although, the latest literature describes more controversial cases, which may increase awareness. Here, we present a rare case of 21 years old female with asymptomatic neck paraganglioma, which was unexpectedly diagnosed after pathological and immunohistochemical testing of removed thyroid gland and showed unusual immunohistochemical variation for SDH mutation.","PeriodicalId":90463,"journal":{"name":"Case reports in clinical pathology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.5430/CRCP.V5N2P5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45691321","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 1

Cellular schwannoma of the breast: A case report and review of literature 乳腺细胞神经鞘瘤1例报告及文献复习

Case reports in clinical pathology Pub Date : 2018-07-09 DOI: 10.5430/CRCP.V5N2P1

Yan Zhang, Hongyi Gao, An-qin Zhang, Jiang-yu Zhang, Kun-he Wu, Yi Wang

引用次数: 1

Hemosiderotic fibrolipomatous tumor: A poorly known entity 含铁血黄素纤维脂肪瘤:一个鲜为人知的实体

Case reports in clinical pathology Pub Date : 2018-06-28 DOI: 10.5430/crcp.v5n1p23

S. Chaieb, M. Njima, N. B. Abdeljelil, A. Bellalah, S. Chouchane, A. Zakhama, A. Moussa

引用次数: 0

Case report of acquired hemophagocytic lymphohistiocytosis associated with progression of monoclonal gammopathy of unknown significance (MGUS) 获得性噬血细胞性淋巴组织细胞增多症伴不明意义单克隆γ病进展1例报告

Case reports in clinical pathology Pub Date : 2018-06-21 DOI: 10.5430/CRCP.V5N1P19

Li Liu, L. Contis, O. Palmer

{"title":"Case report of acquired hemophagocytic lymphohistiocytosis associated with progression of monoclonal gammopathy of unknown significance (MGUS)","authors":"Li Liu, L. Contis, O. Palmer","doi":"10.5430/CRCP.V5N1P19","DOIUrl":"https://doi.org/10.5430/CRCP.V5N1P19","url":null,"abstract":"Background: Acquired hemophagocytic lymphohistiocytosis (HLH) is an aggressive hyperinflammatory syndrome. Without prompt diagnosis and proper treatment, it can be life-threatening. HLH is commonly present in the setting of other autoimmune disorders, infection, organ transplantation, and malignancy. However, to our knowledge, HLH associated with monoclonal gammopathy of undetermined significance (MGUS) has not been reported.Case presentation: A 67-year-old woman with an extensive history of MGUS and renal transplant presented with progressive fatigue, weight loss, intermittent fevers, splenomegaly, and pancytopenia. Serum protein electrophoresis with immunofixation identified a new monoclonal protein IgG lambda and a rapidly increasing pre-existing free kappa light chain. A bone marrow biopsy revealed focal clusters of kappa restricted plasma cells which comprised less than 10% of marrow cellularity. Skeletal survey was negative for osteolytic lesions. She was also free of any end-organ damage. Histological examination showed a prominent increase in histiocytes and macrophages, many of which show erythrophagocytosis and lymphophagocytosis. Together with her clinical presentation along with a hyperferritinemia, a diagnosis of HLH was confirmed utilizing the criteria of the Histiocyte Society. The patient underwent a splenectomy. Prompt treatment with etoposide and high dose dexamethasone eventually stabilized the patient and resulted in a full recovery, which coincided with the disappearance of the serum monoclonal IgG lambda.Conclusions: This report reveals a novel association of HLH with the progression of MGUS. Familiarity with this syndrome and its association with other conditions is indicated to ensure prompt diagnosis and appropriate patient treatment.","PeriodicalId":90463,"journal":{"name":"Case reports in clinical pathology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.5430/CRCP.V5N1P19","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46473346","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Urachal mucinous neoplasms--to be or not to be: Two cases and a review of current diagnostic criteria (WHO 2016) 脐尿管粘液性肿瘤——是或不是：两例病例和当前诊断标准的回顾（世界卫生组织2016）

Case reports in clinical pathology Pub Date : 2018-05-28 DOI: 10.5430/CRCP.V5N1P12

J. Cuadra, L. Pérez, I. García, M. Álvarez, Bernardo Herrera, I. Hierro, L. Vicioso

引用次数: 0