Related ArticlesDermatological and Epidemiological Profiles of Patients with Albinism in São Paulo, Brazil, between 2010 and 2017: A Cross-Sectional Study. Dermatology. 2019 Aug 28;:1-9 Authors: Marçon CR, Moraes JC, de Olivas Ferreira MAM, Oliari CB Abstract INTRODUCTION: Oculocutaneous albinism is an autosomal recessive disease caused by complete absence of or decrease in melanin biosynthesis in melanocytes. Due to the reduction or absence of melanin,...
Thu Aug 29, 2019 14:46
Related ArticlesCharacteristics, combinations, treatments, and survival of second primary hematological neoplasm: a retrospective single-center cohort of 49 patients (Hemo2study). Ann Hematol. 2019 Aug 27;: Authors: Chalopin T, Vallet N, Arbion F, Barin C, Rault E, Villate A, Eloit M, La Rochelle LD, Foucault A, Ertault M, Dartigeas C, Benboubker L, Estienne MH, Domenech J, Hérault O, Gyan E Abstract The coexistence of dual hematological neoplasms is...
Thu Aug 29, 2019 13:15
Related ArticlesPulmonary Carcinosarcoma: A Surveillance, Epidemiology, and End Results (SEER) Analysis. Clin Lung Cancer. 2019 Jul 10;: Authors: Ersek JL, Symanowski JT, Han Y, Howard A, Dumas K, Ahrens W, Kim E, Kim ES Abstract INTRODUCTION: Pulmonary carcinosarcoma (PC) is a rare malignant neoplasm composed of epithelial and mesenchymal components. It accounts for < 1% of thoracic cancers and is not fully understood. This study examined Surveillance,...
Thu Aug 29, 2019 13:15
Related ArticlesBRAF Mutation in Colorectal Rhabdoid and Poorly Differentiated Medullary Carcinomas. Cancers (Basel). 2019 Aug 26;11(9): Authors: Bolzacchini E, Digiacomo N, Marrazzo C, Sahnane N, Maragliano R, Gill A, Albarello L, Sessa F, Furlan D, Capella C Abstract Colorectal rhabdoid carcinomas (CRbCs) are very rare and aggressive cancers. The BRAFmutation and CpG island methylator phenotype have been reported to be common features ofCRbCs. This...
Thu Aug 29, 2019 13:15
Related Articles[The study of the value of H3F3A G34W immunohistochemical staining in the diagnosis of giant cell tumor of bone]. Zhonghua Bing Li Xue Za Zhi. 2019 Jul 08;48(7):531-536 Authors: Bai YQ, Yang TT, Zhang HZ Abstract Objective: To investigate the diagnostic role of H3F3A G34W immunohistochemistry in giant cell tumor of bone. Methods: A total of 275 tumors were collected from 2016 to 2018 at Shanghai Jiaotong University Affiliated Sixth People's...
Thu Aug 29, 2019 13:15
Related Articles[Myxoid lipoblastoma:a clinicopathological study of four cases]. Zhonghua Bing Li Xue Za Zhi. 2019 Jul 08;48(7):527-530 Authors: Zhou J, Li X, Li FC, Zhang JQ, Yang SD Abstract Objective: To study clinicopathological features,diagnosis and differential diagnosis of myxoid lipoblastoma. Methods: Four cases of myxoid lipoblastoma, from 2010 to 2017 at Wuxi People's Hospital of Nanjing Medical University, the Affiliated Hospital of Xuzhou...
Thu Aug 29, 2019 13:15
Related Articles[Clinicopathological observation of adamantinoma of long bone]. Zhonghua Bing Li Xue Za Zhi. 2019 Jul 08;48(7):522-526 Authors: Hua HJ, Li KD, Fang HS, Li H, Zhu Y, Li X, Song GX, Liu C, Zhang ZH, Fan QH Abstract Objective: To investigate the clinicopathological features and differential diagnosis of adamantinoma of long bone. Methods: Seven cases of adamantinoma on long bone were selected at Jiangsu Province People's Hospital from June...
Thu Aug 29, 2019 13:15
Related Articles[A Case of Synchronous Multiple Colon Carcinoma-A Case Report]. Gan To Kagaku Ryoho. 2019 Jun;46(6):1069-1071 Authors: Funamizu N, Sasa Y, Tomori K, Nakabayashi Y Abstract A 67-year-old woman with anemia was referred to us for further study. A colonoscopy exhibited multiple tumors(tub1)in the transverse and sigmoid colon(two regions)and rectum. Contrast-enhanced CT revealed no apparent distant and lymph node metastases. Thus, subtotal...
Thu Aug 29, 2019 13:15
Related Articles[A Case of Histiocytoid Breast Carcinoma Accompanied by Multiple Axillary Lymph Node Metastases]. Gan To Kagaku Ryoho. 2019 Jun;46(6):1049-1051 Authors: Terakawa H, Gabata R, Ishikawa S, Hirata M, Inokuchi M, Kawashima H, Miyashita T, Tajima H, Takamura H, Ninomiya I, Fushida S, Ohta T, Oyama T, Ikeda H Abstract According to previous reports in our country, histiocytoid breast carcinoma is a very rare case of its tissue type, accounting...
Thu Aug 29, 2019 13:15
Related ArticlesIsolated Unilateral Infiltrative Optic Neuropathy in a Patient with Breast Cancer Turk J Ophthalmol. 2019 06 27;49(3):171-174 Authors: Aghdam KA, Zand A, Sanjari MS Abstract Metastasis to the optic nerve is very rare. We report a case of metastatic breast cancer to the optic nerve head without the involvement of other ocular or orbital structures. The patient, a 39-year-old female who had been previously treated for breast cancer, reported...
Thu Aug 29, 2019 13:15
Related Articles[Glioblastoma with BRAFV600E mutation and numerous metastatic foci: a case report]. Folia Neuropathol. 2019;57(1):72-79 Authors: Janik K, Och W, Popeda M, Rosiak K, Peciak J, Rieske P, Kulbacki K, Szostak B, Parda A, Stoczynska-Fidelus E Abstract Glioblastoma, the most malignant astrocytic tumour, is associated with limited survival and thus rare metastases. We analysed a particularly interesting case - a 51-year-old male diagnosed within...
Thu Aug 29, 2019 13:15
Related ArticlesThe epidemiology of central and extraventricular neurocytoma in the United States between 2006 and 2014. J Neurooncol. 2019 May;143(1):123-127 Authors: Tish S, Habboub G, Jones J, Ostrom QT, Kruchko C, Barnholtz-Sloan JS, Recinos PF, Kshettry VR Abstract INTRODUCTION: Central neurocytoma (CN) and extraventricular neurocytoma (EVN) are rare intracranial tumors. There is a paucity of studies reporting the population-based incidence of...
Thu Aug 29, 2019 13:15
Related Articles[Co-occurrence of t(8;21)(q22;q22) and t(9;22)(q34;q11) in a case with chronic myelogenous leukemia]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Mar 10;36(3):253-256 Authors: Gong J, Li J, Gai Y, Tian X, Feng X, Lin Y, Liu E, Ru K Abstract OBJECTIVE: To delineate laboratory and clinical characteristics of a case with chronic myelogenous leukemia (CML) and co-occurrence of t(9;22)(q34;q11) and t(8;21)(q22;q22). METHODS: The patient...
Thu Aug 29, 2019 13:15
Related ArticlesMalignant peripheral nerve sheath tumor (MPNST) arising from angiosarcoma: a rare case report. Oral Maxillofac Surg. 2019 Mar;23(1):109-112 Authors: Lazaridou M, Bourlidou E, Vafeiadou M, Papadiochos Y, Barbetakis N, Kiziridou A, Mangoudi D Abstract PURPOSE: An extremely rare case of divergent differentiation of a cutaneous angiosarcoma to a malignant peripheral nerve sheath tumor (MPNST) is presented. METHODS: A 62-year-old...
Thu Aug 29, 2019 13:15
Related ArticlesAdenoid Cystic Carcinoma With Sialolithiasis of the Left Submandibular Gland: A Case Report and Literature Review. Int J Surg Pathol. 2019 May;27(3):305-310 Authors: Miyabe S, Ishibashi K, Saida K, Fujiyoshi Y, Fukano H, Ueda K, Ueda S, Watanabe S, Nagao T Abstract Adenoid cystic carcinoma is one of the most common salivary gland malignancies with poor long-term prognosis, but the coexistence of sialoliths is extraordinarily rare. In...
Thu Aug 29, 2019 13:15
Related ArticlesSynchronous Pulmonary Adenofibroma and Solitary Fibrous Tumor: Case Report and Review of the Literature. Int J Surg Pathol. 2019 May;27(3):322-327 Authors: Olson NJ, Czum JM, de Abreu FB, Linos K, Black CC Abstract Pulmonary adenofibroma (PAF) is a rare neoplasm that may be related to solitary fibrous tumor (SFT). A subset of PAFs harbor the NAB2-STAT6 fusion that is typical of SFT, but a significant proportion do not. Their distinction...
Thu Aug 29, 2019 13:15
Related ArticlesPharmacokinetic evaluation of the PNC disassembler metarrestin in wild-type and Pdx1-Cre;LSL-KrasG12D/+;Tp53R172H/+ (KPC) mice, a genetically engineered model of pancreatic cancer. Cancer Chemother Pharmacol. 2018 12;82(6):1067-1080 Authors: Vilimas T, Wang AQ, Patnaik S, Hughes EA, Singleton MD, Knotts Z, Li D, Frankowski K, Schlomer JJ, Guerin TM, Springer S, Drennan C, Dextras C, Wang C, Gilbert D, Southall N, Ferrer M, Huang S, Kozlov S, Marugan...
Thu Aug 29, 2019 13:15
Related ArticlesCombined Sclerosing and Spindle Cell Rhabdomyosarcoma in Previous Craniotomy Site: A Case Report and a Review of the Literature. Int J Surg Pathol. 2019 May;27(3):328-335 Authors: Gui H, Lhospital E, Staddon AP, Nagda SN, Zager EL, Zhang PJL, Brooks JS Abstract Sclerosing rhabdomyosarcoma (RMS) is a rare subtype of RMS with unique prominent stromal hyalinization and a pseudovascular architecture. It overlaps morphologically with spindle...
Thu Aug 29, 2019 13:15
Related ArticlesPolyethylenimine-Spherical Nucleic Acid Nanoparticles against Gli1 Reduce the Chemoresistance and Stemness of Glioblastoma Cells. Mol Pharm. 2018 11 05;15(11):5135-5145 Authors: Melamed JR, Ioele SA, Hannum AJ, Ullman VM, Day ES Abstract Glioblastoma (GBM) is the most common and lethal primary brain tumor in adults, with nearly 100% of patients ultimately succumbing to the disease. Median patient survival is 15 months, and no standard...
Thu Aug 29, 2019 13:15
Related ArticlesComposite Paraganglioma: Pioneering in the Head and Neck. Int J Surg Pathol. 2019 May;27(3):282-289 Authors: Delgado S, Smith SM, Mehra S, Prasad ML Abstract Composite paragangliomas are rare with less than 20 cases documented in the abdomen, retroperitoneum, and urinary bladder. In this article, we report the first case of composite paraganglioma in the head and neck presenting as a soft tissue mass in the neck adjacent to the carotid...
Thu Aug 29, 2019 13:15
Related ArticlesParathyroid Carcinoma Causing Mild Hyperparathyroidism in Neurofibromatosis Type 1: A Case Report and Systematic Review. Endocr Metab Immune Disord Drug Targets. 2019;19(3):382-388 Authors: Triggiani V, Castellana M, Basile P, Renzulli G, Giagulli VA Abstract BACKGROUND: Neurofibromatosis type 1 is an autosomal dominant disorder characterized by an increased incidence of tumors, including endocrine ones. Primary hyperparathyroidism...
Thu Aug 29, 2019 13:15
Related ArticlesEndometriosis With Cystic Degeneration: A Rare Disease of Males. Int J Surg Pathol. 2019 May;27(3):311-314 Authors: Al-Obaidy KI, Idrees MT Abstract Endometriosis in men is extremely rare with only a few cases reported in the English literature. Different theories have been proposed as to its origin. In this article, we describe the clinicopathologic features of 2 cases of endometriosis occurring in male patients. The patients' ages...
Thu Aug 29, 2019 13:15
Related ArticlesCribriform-Morular Variant of Papillary Thyroid Carcinoma With Poorly Differentiated Features: A Case Report With Immunohistochemical and Molecular Genetic Analysis. Int J Surg Pathol. 2019 May;27(3):294-304 Authors: Corean J, Furtado LV, Kadri S, Segal JP, Emerson LL Abstract Cribriform-morular variant of papillary thyroid carcinoma (CMVPTC) is usually an inherited malignancy and may be a presenting indicator of familial adenomatous...
Thu Aug 29, 2019 13:15
Related ArticlesNeuroendocrine Tumor Arising in a Tailgut Cyst: A Rare Presacral Tumor. Int J Surg Pathol. 2019 May;27(3):336-342 Authors: Iwata E, Orosz Z, Teh J, Reynolds J, Whitwell D, Tanaka Y, Athanasou NA Abstract A tailgut cyst (retrorectal cystic hamartoma) is an uncommon lesion that develops in the presacral (retrorectal) space. Malignant change in a tailgut cyst is extremely rare and presents as a soft tissue (presacral) or bone (sacral) neoplasm....
Thu Aug 29, 2019 13:15
Related Articles"Z4" Complex Member Fusions in NUT Carcinoma: Implications for a Novel Oncogenic Mechanism. Mol Cancer Res. 2018 12;16(12):1826-1833 Authors: Shiota H, Elya JE, Alekseyenko AA, Chou PM, Gorman SA, Barbash O, Becht K, Danga K, Kuroda MI, Nardi V, French CA Abstract Nuclear protein in testis (NUT) carcinoma (NC) is a rare, distinctly aggressive subtype of squamous carcinoma defined by the presence of NUT-fusion oncogenes resulting from...
Thu Aug 29, 2019 13:15
Related ArticlesPulmonary Carcinomas With Mucinous and Neuroendocrine Differentiation: Expanding the Spectrum of Amphicrine Carcinomas. Am J Surg Pathol. 2018 09;42(9):1246-1252 Authors: Weissferdt A Abstract Amphicrine carcinoma is a distinct type of carcinoma characterized by synchronous exocrine and endocrine differentiation within the same tumor cell. Such tumors are exceedingly rare and most commonly recognized in the gastrointestinal tract. In...
Thu Aug 29, 2019 13:15
Related ArticlesCutaneous Non-Neural Granular Cell Tumors Harbor Recurrent ALK Gene Fusions. Am J Surg Pathol. 2018 09;42(9):1133-1142 Authors: Cohen JN, Yeh I, Jordan RC, Wolsky RJ, Horvai AE, McCalmont TH, LeBoit PE Abstract Non-neural granular cell tumor (NNGCT; also known as primitive polypoid granular cell tumor) is a rare neoplasm composed of large ovoid cells with abundant granular cytoplasm, variable nuclear pleomorphism, and the potential for...
Thu Aug 29, 2019 13:15
Related ArticlesRadiation Therapy in Ovarian Cancer: An Overview and Future Directions. Clin Oncol (R Coll Radiol). 2018 08;30(8):504-506 Authors: McCormack M Abstract Clear cell cancer of the ovary is a rare and aggressive subtype. There is a general paucity of data from randomised trials to inform the most appropriate approach to adjuvant therapy. Retrospective data has highlighted an improvement in disease free survival with the addition of whole...
Thu Aug 29, 2019 13:15
Related ArticlesPoorly Differentiated Nonkeratinizing Squamous Cell Carcinoma of the Thymus: Clinicopathologic and Molecular Genetic Study of 25 Cases. Am J Surg Pathol. 2018 09;42(9):1224-1236 Authors: Suster D, Pihan G, Mackinnon AC, Suster S Abstract Thymic carcinoma represents a rare and poorly understood type of thymic epithelial neoplasm that has been the subject of much controversy. Poorly differentiated nonkeratinizing squamous cell carcinoma,...
Thu Aug 29, 2019 13:15
Related ArticlesAdenocarcinoma of the oesophagus: neoadjuvant chemoradiation and radical surgery : Long-term results. Strahlenther Onkol. 2018 11;194(11):1007-1016 Authors: Vitz S, Göbel H, Leibl B, Aigner T, Grabenbauer GG Abstract PURPOSE: To retrospectively evaluate long-term treatment results following neoadjuvant chemoradiation (CRT) and radical surgery in patients with advanced adenocarcinoma (AC) of the oesophagus. PATIENTS AND METHODS:...
Thu Aug 29, 2019 13:15
Related Articles[Laryngeal papillomatosis: A rare cause of dysphonia in the child. Case series]. Arch Argent Pediatr. 2018 06 01;116(3):e471-e475 Authors: Cuestas G, Rodríguez V, Doormann F, Bellia Munzón P, Bellia Munzón G Abstract Juvenile laryngeal papillomatosis is an uncommon disease caused by human papilloma virus, mainly types 6 and 11. It is the most common benign laryngeal tumor in children. This condition should be suspected in any children...
Thu Aug 29, 2019 13:15
Related ArticlesStevens-Johnson Syndrome associated with methotrexate treatment for acute lymphoblastic leukemia: a case report. Arch Argent Pediatr. 2018 06 01;116(3):e459-e462 Authors: Akıncı B, Siviş ZÖ, Şahin A, Karapınar DY, Balkan C, Kavaklı K, Aydınok Y Abstract Toxic epidermal necrolysis and Stevens-Johnson syndrome are rare mucocutaneous diseases which are associated with a prolonged course and potentially lethal outcome. They are mostly drug...
Thu Aug 29, 2019 13:15
Related Articles[A rare differential diagnosis of jugulotympanic paraganglioma]. Laryngorhinootologie. 2018 01;97(1):47-49 Authors: Höhn E, Aschendorff A, Arndt S, Elsheikh S, Jakob TF PMID: 29036733 [PubMed - indexed for MEDLINE]
Thu Aug 29, 2019 13:15
Related ArticlesSociodemographic Predictors of Anal Cancer Screening and Follow-up in Human Immunodeficiency Virus-Infected Individuals. Cancer Nurs. 2018 Sep/Oct;41(5):424-430 Authors: Wells JS, Holstad MM, Watkins Bruner D Abstract BACKGROUND: Anal cancer in the United States is generally rare; however, human immunodeficiency virus (HIV)-infected individuals are 28 times more likely to be given a diagnosis of anal cancer than the general population....
Thu Aug 29, 2019 13:15
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