Related ArticlesLong-term survival after surgical treatment followed by adjuvant systemic therapy for primary duodenal melanoma. Clin J Gastroenterol. 2020 Mar 20;: Authors: Surjan RCT, do Prado Silveira S, Dos Santos ES, de Meirelles LR Abstract Primary mucosal malignant melanomas of the gastrointestinal tract are rare tumors associated to poor prognosis. Primary duodenal involvement by pigmented lesions is even more uncommon, and only a few reports...
Related ArticlesManeuvering the Management of a Rare Case of Primary Undifferentiated Cardiac Sarcoma. Am J Case Rep. 2020 Mar 21;21:e918878 Authors: Abbas HA, Amini B, Wang WL, Ravi V Abstract BACKGROUND Primary cardiac tumors are rare and mostly benign. Cardiac sarcomas are the most common malignant neoplasms of the heart and harbor a dismal prognosis of 6 to 12 months. The diagnosis of cardiac sarcomas may be challenging. Treatment entails surgical...
Related ArticlesCryptic and atypical KMT2A-USP2 and KMT2A-USP8 rearrangements identified by mate pair sequencing in infant and childhood leukemia. Genes Chromosomes Cancer. 2020 Mar 20;: Authors: Blackburn PR, Smadbeck JB, Znoyko I, Webley MR, Pitel BA, Vasmatzis G, Xu X, Greipp PT, Hoppman NL, Ketterling RP, Baughn LB, Lindsey KG, Schandl CA, Wolff DJ, Peterson JF Abstract Infant leukemias are a rare group of neoplasms that are clinically and biologically...
Related ArticlesFatal pediatric Stevens-Johnson syndrome/toxic epidermal necrolysis: Three case reports. Medicine (Baltimore). 2020 Mar;99(12):e19431 Authors: Shi T, Chen H, Huang L, Fan H, Yang D, Zhang D, Lu G Abstract RATIONALE: Stevens-Johnson syndrome and toxic epidermal necrolysis (SJS/TEN) are extremely rare but potentially life-threatening disorders. We presented 3 fatal pediatric SJS/TEN cases. PATIENT CONCERNS: Our patients had some...
Related ArticlesIsolated DHEAS production by an adrenal neoplasm: Clinical, biochemical and pathologic characteristics. Urol Case Rep. 2020 Jul;31:101148 Authors: Pingle SR, Jalil F, Millar D, Malchoff CD, Ristau BT Abstract Androgen-secreting adrenal neoplasms have a low incidence, usually secrete multiple hormones, and may present with hirsutism, acne, and alopecia. We report an exceedingly rare case of a purely dehydroepiandrosterone-sulfate (DHEA-S)...
Related ArticlesThe Use of Genomics To Drive Kidney Disease Drug Discovery and Development. Clin J Am Soc Nephrol. 2020 Mar 19;: Authors: Reilly DF, Breyer MD Abstract As opposed to diseases such as cancer, autoimmune disease, and diabetes, identifying drugs to treat CKD has proven significantly more challenging. Over the past two decades, new potential therapeutic targets have been identified as genetically altered proteins involved in rare monogenetic...
Related ArticlesSynchronic renal cell carcinoma associated with fibromixoid sarcoma: A rare finding. Int J Surg Case Rep. 2020 Feb 28;68:214-217 Authors: Ribeiro JGA, Fosse Junior ÂM, Frade VB, Rocha GG, Pires LAS, Souza CFC, Babinski MA Abstract INTRODUCTION: Renal cell carcinoma comprises over 90% of renal cancers, thus, it is the most common form of renal neoplasia. This carcinoma can often present itself in a variable fashion, ranging from incidentalomas...
Related Articles[Hereditary predispositions to follicular thyroid tumors]. Ann Pathol. 2020 Mar 16;: Authors: Decaussin-Petrucci M Abstract Familial thyroid cancers of follicular origin are rare and include syndromic and non-syndromic tumours. In familial adenomatous polyposis, the prevalence of papillary thyroid cancer is 2-12% and in 20-40% of cases it is a cribriform-morular papillary thyroid carcinoma. Morules and cribriform pattern are the two main...
Related ArticlesSeminal Vesicle Involvement by Carcinoma In Situ of the Bladder: Clonal Analysis Using Next-Generation Sequencing to Elucidate the Mechanism of Tumor Spread. Cancer Res Treat. 2020 Mar 19;: Authors: Park HS, Shin H, Lee MS, Kim JH, Kim SY, Park J Abstract We present a rare case of urothelial carcinoma in situ (CIS), which invades the prostate and seminal vesicle (SV). A 70-year-old man underwent transurethral resection of bladder (TURB),...
Related ArticlesPathologically confirmed brain metastases from primary uterine cervical tumors: two cases and a literature review. World J Surg Oncol. 2019 Oct 31;17(1):174 Authors: Bi Y, Li L Abstract BACKGROUND: Pathologically confirmed brain metastasis from primary cervical cancer is extremely rare. Herein, we report two cases of intracranial metastasis from cervical cancer that were histopathologically confirmed after surgical excision. In addition,...
Related ArticlesSolitary metastasis of myxoid liposarcoma from the thigh to intraperitoneum: a case report. World J Surg Oncol. 2019 Oct 28;17(1):172 Authors: Kim DW, Jee YS Abstract BACKGROUND: The purpose of case report was to present a rare case of a solitary metastasis of myxoid liposarcoma and discuss the clinical and pathological information for patients treated for metastatic myxoid liposarcoma. CASE PRESENTATION: We report our experience...
Related ArticlesCystic lymphangioma in the peripheral jejunal mesentery in an adult and excision with laparoscopic-assisted surgery: a case report. World J Surg Oncol. 2019 Oct 24;17(1):170 Authors: Nagano H, Kimura T, Iida A, Togawa T, Goi T, Sato Y Abstract BACKGROUND: Lymphangiomas are uncommon congenital malformations that present mainly in the head, neck, and axillar regions in pediatric patients. Mesenteric cystic lymphangiomas (MCLs), which...
Related ArticlesCharacteristics of CD5-positive diffuse large B-cell lymphoma among Koreans: High incidence of BCL2 and MYC double-expressors. PLoS One. 2019;14(10):e0224247 Authors: Na HY, Choe JY, Shin SA, Kim HJ, Han JH, Kim HK, Oh SH, Kim JE Abstract Aberrant expression of CD5 has been reported in 5-10% of diffuse large B-cell lymphomas (DLBCLs). CD5+ DLBCL had been recognized as an aggressive immunophenotypic subgroup of DLBCL in the 2008 WHO...
Related ArticlesThe infectious thyroid nodule: a case report of mucormycosis associated with ibrutinib therapy. J Otolaryngol Head Neck Surg. 2019 Oct 16;48(1):49 Authors: Mascarella MA, Schweitzer L, Alreefi M, Silver J, Caglar D, Loo VG, Richardson K, Dufresne P, Lee TC, Sadeghi N Abstract BACKGROUND: Acute invasive fungal infections of the head and neck secondary to tyrosine kinase inhibitors are rare and potentially life-threatening events. ...
Related ArticlesAntrodia Cinnamomea Prolongs Survival in a Patient with Small Cell Lung Cancer. Medicina (Kaunas). 2019 Sep 26;55(10): Authors: Long H, Hu CT, Weng CF Abstract Introduction: Antrodia cinnamomea (AC) is an extremely rare medicinal fungus native to forested regions of Taiwan. It possesses numerous biological activities, especially anti-tumor effects shown in various in vitro cancer cells and in vivo animal models. However, there are few...
Related ArticlesPrimary and secondary breast angiosarcoma: single center report and a meta-analysis. Breast Cancer Res Treat. 2019 Dec;178(3):523-533 Authors: Abdou Y, Elkhanany A, Attwood K, Ji W, Takabe K, Opyrchal M Abstract BACKGROUND: Primary and secondary breast angiosarcoma is a rare and aggressive malignancy with limited published literature. Optimal management is mostly based on expert opinion. Our study aims to describe a single institution...
Related ArticlesA Rapidly Enlarging Neck Mass: A Case Report. Am J Med. 2019 12;132(12):e858-e859 Authors: Moale A, Zimmerman J PMID: 31326410 [PubMed - indexed for MEDLINE]
Related ArticlesLong-Term Results of Bilateral Lung Transplantation in Patients With End-Stage Pulmonary Lymphangioleiomyomatosis. Prog Transplant. 2019 06;29(2):115-121 Authors: Salman J, Ius F, Sommer W, Siemeni T, Fleissner F, Alhadidi H, Kugler C, Avsar M, Haverich A, Warnecke G, Tudorache I, Kuhn C Abstract INTRODUCTION: Lymphangioleiomyomatosis (LAM) is a rare disease in women, leading to progressive deterioration of lung function and respiratory...
Related ArticlesA Practical Guide for the Production and PET/CT Imaging of 68Ga-DOTATATE for Neuroendocrine Tumors in Daily Clinical Practice. J Vis Exp. 2019 04 17;(146): Authors: Aalbersberg EA, Geluk-Jonker MM, Young-Mylvaganan T, de Wit-van der Veen LJ, Stokkel MPM Abstract Neuroendocrine tumors are a rare form of cancer that arise from neuroendocrine cells and can be present at almost any location throughout the body. Although heterogeneous in...
Related ArticlesChyle Leak Following Autologous Breast Reconstruction: A Rare Complication of a Deep Inferior Epigastric Artery Perforator Flap. Ann Plast Surg. 2019 02;82(2):193-195 Authors: Long SR, Butterworth JA Abstract BACKGROUND: While complications of deep inferior epigastric artery perforator flaps are known and well documented, a thorough literature review revealed no other reports of a patient developing a chyle leak following the use of...
Related ArticlesClinical Benefit to an Aurora A Kinase Inhibitor in a Patient with Metastatic Integrase Interactor 1-Deficient Carcinoma. Oncologist. 2019 02;24(2):146-150 Authors: Karantanos T, Rooper L, Kang Y, Lin CT, Wenga P, Sagorsky S, Lauring J, Kang H Abstract Integrase interactor 1 (INI-1)-deficient carcinoma is a rare cancer characterized by the loss of the SWItch/Sucrose Non-Fermentable-related matrix-associated actin-dependent regulator...
Related ArticlesAcute promyelocytic leukemia in patients aged >70 years is not rare and highly curable: a single center series of 21 unselected patients. Leuk Lymphoma. 2019 02;60(2):531-534 Authors: Borlenghi E, Cattaneo C, Schieppati F, Gramegna D, Passi A, Rossi G PMID: 30160625 [PubMed - indexed for MEDLINE]
Related ArticlesA Different Perspective on Breast Implant Surface Texturization and Anaplastic Large Cell Lymphoma (ALCL). Aesthet Surg J. 2019 01 01;39(1):56-63 Authors: Brown T, Harvie F, Stewart S Abstract Anaplastic large cell lymphoma (ALCL) is a rare form of lymphoma involving cells of the immune system. It is currently gaining interest because of an association between the development of ALCL and an increased risk in women who have had breast...
Related ArticlesGenomic and pathological heterogeneity in clinically diagnosed small cell lung cancer in never/light smokers identifies therapeutically targetable alterations. Mol Oncol. 2020 Mar 19;: Authors: Ogino A, Choi J, Lin M, Wilkens MK, Calles A, Xu M, Adeni AE, Chambers ES, Capelletti M, Butaney M, Gray NS, Gokhale PC, Palakurthi S, Kirschmeier P, Oxnard GR, Sholl LM, Jänne PA Abstract Small cell lung cancer (SCLC) occurs infrequently in never/former...
Related Articles[Perioperative management of paragangliomas and pheochromocytomas]. Medwave. 2020 Mar 04;20(2):e7830 Authors: Fermandois M, Altamirano J, Rojas F, Román C, Pinto I Abstract Pheochromocytomas and paragangliomas are rare neuroendocrine tumors, characterized by a high morbidity rate due to catecholamine excess. These high levels are independent of physiologic stressors. For the diagnosis, a biochemical workup is paramount. The most widely...
Related ArticlesCombining surgery with 125I brachytherapy for recurrent mediastinal dedifferentiated liposarcoma: A case report and review of literature. World J Clin Cases. 2020 Mar 06;8(5):939-945 Authors: Chen HG, Zhang K, Wu WB, Wu YH, Zhang J, Gu LJ, Li XJ Abstract BACKGROUND: Dedifferentiated liposarcoma in the mediastinum is an extremely rare malignant neoplasm. A few previous case reports indicate that surgical resection is the major treatment,...
Related ArticlesMultiple Primary Malignant Neoplasms: An Unusual Case of Metachronous Breast Ductal and Squamous Cell Carcinomas. Cureus. 2020 Feb 11;12(2):e6954 Authors: Ibrahim ME, Saleh M, Ali A, Alavi N Abstract Multiple primary malignant neoplasms (MPMN) are generally defined as the co-occurrence of multiple primary malignant neoplasms of distinct histology in the same individual. Second and higher-order primary malignancies now comprise about 18%...
Related ArticlesAbdominal wall schwannoma: a case report. Gastroenterol Hepatol Bed Bench. 2020;13(1):95-100 Authors: Tarchouli M, Essarghini M, Qamouss O, El Kharras A, Bounaim A Abstract Schwannomas or neurilemmomas are benign and slow-growing tumors that arise exclusively from Schwann cells in peripheral nerve sheaths. These neoplasms theoretically can occur anywhere in the body, but they most frequently affect extremities, as well as head and neck...
Related ArticlesClinicopathological Features of Advanced Gastric Cancers which Were Misjudged and Subjected to Endoscopic Submucosal Dissection. Gastroenterol Res Pract. 2020;2020:6525098 Authors: Ochiai Y, Kikuchi D, Inoshita N, Hayasaka J, Suzuki Y, Tanaka M, Nomura K, Odagiri H, Yamashita S, Matsui A, Iizuka T, Kitagawa M, Hoteya S Abstract Background and Aims: Endoscopic submucosal dissection (ESD) is widely performed for early gastric cancer (EGC)....
Related ArticlesHead-to-head comparison of [18F]-fluorodeoxyglucose and [18F]-fluorocholine positron emission tomography/computed tomography in three patients with rare gestational trophoblastic neoplasms: A case series. World J Nucl Med. 2020 Jan-Mar;19(1):72-77 Authors: Thientunyakit T, Thongpraparn T, Siriprapa T, Gelovani JG Abstract We report the efficacy of dual positron emission tomography/computed tomography (PET/CT) imaging with [18F]-2'-fluoro-2'-deoxy-D-glucose...
Related ArticlesPrimary intraosseous adenoid cystic carcinoma of the mandible: A rare clinical entity. J Oral Maxillofac Pathol. 2020 Feb;24(Suppl 1):S42-S45 Authors: Reddy V, Wadhwan V, Arunkumar KV, Venkatesh A Abstract Central intraosseous adenoid cystic carcinoma (ACC) of the mandible, formerly known as cylindroma, is a rare neoplasm with only 47 cases reported in the literature. We present a case of central ACC involving the mandible of a 55-year-old...
Related ArticlesPhase 2 study of pembrolizumab in patients with advanced rare cancers. J Immunother Cancer. 2020 Mar;8(1): Authors: Naing A, Meric-Bernstam F, Stephen B, Karp DD, Hajjar J, Rodon Ahnert J, Piha-Paul SA, Colen RR, Jimenez C, Raghav KP, Ferrarotto R, Tu SM, Campbell M, Wang L, Sabir SH, Tapia C, Bernatchez C, Frumovitz M, Tannir N, Ravi V, Khan S, Painter JM, Abonofal A, Gong J, Alshawa A, McQuinn LM, Xu M, Ahmed S, Subbiah V, Hong DS, Pant S, Yap TA, Tsimberidou...
Related ArticlesExtraskeletal chondrosarcoma in the tongue of a dog: case report and retrospective analysis of 236 tongue masses (2011-2019). J Vet Diagn Invest. 2020 Mar 19;:1040638720911394 Authors: Rahe MC, Westegaard T, Yaeger M Abstract Chondrosarcomas are common tumors of the canine appendicular and axial skeleton; however, extraskeletal chondrosarcomas are very rare. Herein we report a case of extraskeletal chondrosarcoma in the tongue of a dog....
Related Articles[Priority setting in scaled-up cancer screening in China: an systematic review of economic evaluation evidences]. Zhonghua Yu Fang Yi Xue Za Zhi. 2020 Mar 06;54(3):306-313 Authors: Shi JF, Mao AY, Bai YN, Liu GX, Liu CC, Wang H, Cao MM, Feng H, Wang L, Bai FZ, Huang HY, Bai HJ, Zhu J, Yan XX, Zhang J, Ren JS, Li N, Dai M, Chen WQ Abstract Objective: The existed economic evaluations of cancer screening in Chinese population are almost...
Related Articles[Renal angiomyolipoma with epithelial cysts: a clinicopathological analysis of four cases]. Zhonghua Bing Li Xue Za Zhi. 2020 Mar 08;49(3):244-249 Authors: Zhang X, He XL, Zhao M Abstract Objective: To investigate the clinicopathological features,diagnosis and differential diagnosis of renal angiomyolipoma with epithelial cysts(AMLEC). Methods: Four cases of renal AMLEC diagnosed between January 2014 and June 2019 at the Department of...
Related Articles[Thyrotropin-secreting pituitary adenoma]. Orv Hetil. 2020 Mar;161(12):474-478 Authors: Sohár G, Györkös A, Dóczi T, Kajtár B, Piski Z, Kovács M Abstract Thyrotropin-secreting pituitary tumors are rare causes of hyperthyroidism and account for less than 1% of all pituitary adenomas. The number of reported cases increased over the last few years as a consequence of the routine use of ultrasensitive immunometric assays for measuring thyrotropin...
Related ArticlesPredictors of Outcome in Patients With Fibrolamellar Carcinoma: Analysis of the National Cancer Database. Anticancer Res. 2020 Feb;40(2):847-855 Authors: Assi HA, Mukherjee S, Machiorlatti M, Vesely S, Pareek V, Hatoum H Abstract BACKGROUND: Fibrolamellar carcinoma (FLC) is a very rare liver tumor. We aimed to retrospectively analyze the clinicopathological factors and treatment modalities affecting overall survival (OS) in FLC. The...
Related ArticlesEstablishment and Characterization of a Novel Primitive Yolk Sac Tumour Cell Line, TC587. Anticancer Res. 2020 Feb;40(2):759-766 Authors: Iwasaki T, Kohashi K, Ohno M, Taguchi T, Oda Y Abstract BACKGROUND/AIM: Yolk sac tumour (YST) is a rare malignant ovarian germ cell tumour that often occurs in young women or adolescents and exhibits an unfavourable outcome. To evaluate the biological behavior of carcinomas in vitro, permanent tumour...
Related ArticlesSystemic lupus erythematosus associated with thymoma: A fifteen-year observational study in France. Autoimmun Rev. 2020 Mar;19(3):102464 Authors: Noël N, Le Roy A, Hot A, Saadoun D, Lazaro E, Lévesque H, Le Gouellec N, Meaux-Ruault N, Nguyen T, Costedoat-Chalumeau N, Amieux B, Fontana A, De Gennes C, Fulpin J, Thomas PA, Bluthgen MV, Besse B, Lambotte O Abstract OBJECTIVE: To describe the clinical, biological and pathological characteristics...
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