Pathogenic ATM Mutations in Cancer and a Genetic Basis for Radiotherapeutic Efficacy. J Natl Cancer Inst. 2020 Jul 29;: Authors: Pitter KL, Casey DL, Lu YC, Hannum M, Zhang Z, Song X, Pecorari I, McMillan B, Ma J, Samstein RM, Pei IX, Khan AJ, Braunstein LZ, Morris LGT, Barker CA, Rimner A, Alektiar KM, Romesser PB, Crane CH, Yahalom J, Zelefsky MJ, Scher HI, Bernstein JL, Mandelker DL, Weigelt B, Reis-Filho JS, Lee NY, Powell SN, Chan TA, Riaz N, Setton J ...
Thu Jul 30, 2020 13:01
Related Articles Novel Biomarkers in Sinonasal Cancers: from Bench to Bedside. Curr Oncol Rep. 2020 Jul 29;22(10):106 Authors: Lechner M, Liu J, Lund VJ Abstract PURPOSE OF REVIEW: Sinonasal cancers are a heterogenous group of rare cancers for which histopathological diagnosis can be very challenging and treatment options are limited for advanced disease in particular. Here, we review the candidacy of novel diagnostic and prognostic biomarkers,...
Thu Jul 30, 2020 13:01
Related Articles Intrapancreatic Accessory Spleen: Two Case Reports of a Rare Entity. Cureus. 2020 Jun 24;12(6):e8797 Authors: Kykalos S, Machairas N, Molmenti EP, Sotiropoulos G Abstract Intrapancreatic accessory splenic tissue constitutes a very unusual anatomical variation. It is encountered mostly in the splenic hilum or within the pancreatic tail. Given the diagnostic difficulty in excluding a pancreatic malignancy, a distal pancreatectomy...
Thu Jul 30, 2020 13:01
Related Articles Case Report: Primary melanoma of the gastroesophageal junction. F1000Res. 2020;9:490 Authors: Hussein Agha Y, Parker NA, Alderson J Abstract Primary malignant melanoma represents the fifth most common cancer in the United States. It is subdivided into two forms: cutaneous (90%), visceral (8%, including ocular and mucosal) and of unknown primary (2%). The vast majority of gastrointestinal melanomas are secondary lesions until...
Thu Jul 30, 2020 13:01
Related Articles FROM ERECTILE DYSFUNCTION TO BRAIN SUBEPENDYMOMA: A CASE REPORT. Acta Clin Croat. 2020 Mar;59(1):173-176 Authors: Bačun T, Kibel A, Degmečić D, Pavić R Abstract Endocrinopathies are relatively rare causes of erectile dysfunction. Cases of hyperprolactinemia and pituitary adenomas have been previously reported. We present a clinical case of a 27-year-old male with suspected infertility and recent symptoms of erectile dysfunction....
Thu Jul 30, 2020 13:01
Related Articles ETV6-ACSL6 fusion gene in myeloid neoplasms: clinical spectrum, current practice, and outcomes. Orphanet J Rare Dis. 2020 Jul 28;15(1):192 Authors: Wu X, Cai H, Qiu Y, Li J, Zhou DB, Cao XX Abstract BACKGROUND: ETV6-ACSL6 is a fusion gene rarely reported in myeloid malignancies, and its clinical characteristics, proper treatment strategies, and effect on prognosis are poorly understood. RESULTS: Sixteen patients with...
Thu Jul 30, 2020 13:01
Related Articles Clinicopathological and Imaging Features Predictive of Clinical Outcome in Metaplastic Breast Cancer. Curr Med Imaging. 2020;16(6):729-738 Authors: Yoon GY, Cha JH, Kim HH, Shin HJ, Chae EY, Choi WJ, Oh HY Abstract BACKGROUND: Metaplastic breast cancer (MC) is a rare disease, thus it is difficult to study its clinical outcomes. OBJECTIVES: To investigate whether any clinicopathological or imaging features were associated...
Thu Jul 30, 2020 13:01
Related Articles [Radical nephrectomy and partial nephrectomy]. Aktuelle Urol. 2020 Jul 28;: Authors: Eich C, Giessing M Abstract Renal cell carcinoma is the 2nd most frequent urological malignancy in women and the third most frequent in men, with an age peak in the seventh decade of life. If detected early in a local non-metastatic stage, options for complete recovery are excellent. While two decades ago, even locally limited cancers of the...
Thu Jul 30, 2020 13:01
Related Articles Primary Driver Mutations in GTF2I Specific to the Development of Thymomas. Cancers (Basel). 2020 Jul 24;12(8): Authors: Higuchi R, Goto T, Hirotsu Y, Yokoyama Y, Nakagomi T, Otake S, Amemiya K, Oyama T, Mochizuki H, Omata M Abstract Thymomas are rare mediastinal tumors that are difficult to treat and pose a major public health concern. Identifying mutations in target genes is vital for the development of novel therapeutic strategies....
Thu Jul 30, 2020 13:01
Related Articles Laparoscopic management of gastric liposarcoma: A case report and review of the literature. Int J Surg Case Rep. 2020 Jul 18;73:268-270 Authors: Jalal HWC, Gómez D, Pedraza M, Bulicie HC, Cabrera LF, Gil LPG, Acevedo D, Cabrera L, Moreno V, Mendoza A Abstract INTRODUCTION: Liposarcoma is one of the most common mesenchymal neoplasms in adults. Predominant locations are the retroperitoneum and limbs, it rarely occurs in the gastrointestinal...
Thu Jul 30, 2020 13:01
Related Articles Pre-treatment CT imaging in stage IIIA lung cancer: Can we predict local recurrence after definitive chemoradiotherapy? Clin Imaging. 2020 Jul 17;69:133-138 Authors: Plodkowski AJ, Araujo-Filho JAB, Simmers CDA, Girshman J, Raj M, Zheng J, Rimner A, Ginsberg MS Abstract OBJECTIVES: The aim of this study was to delineate computed tomography (CT) features of stage IIIA non-small cell lung cancers on pre-treatment staging studies...
Thu Jul 30, 2020 13:01
Related Articles [Malignant Solitary Fibrous Tumor of the Pleura;Report of a Case]. Kyobu Geka. 2020 May;73(5):392-395 Authors: Ohsawa F, Kamiyoshihara M, Yoshikawa R, Yazawa T, Matsuura N, Igai H Abstract We report a rare case of a malignant solitary fibrous tumor of the pleura(SFTP). The patient was a 66-year-old man, who had an asymptomatic 25 mm nodule in the left upper lung field. We performed a wedge resection of the left lung by video-assisted...
Thu Jul 30, 2020 13:01
Related Articles Management and Reconstruction of a Massive Neonatal Neck Teratoma. J Craniofac Surg. 2020 May/Jun;31(3):e254-e256 Authors: Aivaz M, Manrique M, Bryant JR, Mantilla-Rivas E, Oh AK, Rogers GF, Boyajian MJ Abstract Cervical teratoma is a rare tumor comprised of multiple tissue types. These masses can result in significant functional and aesthetic complications, and surgical intervention is the mainstay of treatment. The authors...
Thu Jul 30, 2020 13:01
Related Articles [Recurrent High-grade Astroblastoma Treated with Stereotactic Radiotherapy:A Case Report]. No Shinkei Geka. 2020 Feb;48(2):151-158 Authors: Higuchi S, Kawanishi Y, Kondo Y, Nakai E, Fukuda H, Fukui N, Nakajo T, Kobayashi K, Murakami I, Ueba T Abstract INTRODUCTION: Astroblastoma is a rare, supratentorial glial tumor, occurring predominantly in children and young adults. However, treatment strategies have not yet been established...
Thu Jul 30, 2020 13:01
Related Articles Inflammatory leiomyosarcoma shows frequent co-expression of smooth and skeletal muscle markers supporting a primitive myogenic phenotype: a report of 9 cases with a proposal for reclassification as low-grade inflammatory myogenic tumor. Virchows Arch. 2020 Aug;477(2):219-230 Authors: Michal M, Rubin BP, Kazakov DV, Michalová K, Šteiner P, Grossmann P, Hájková V, Martínek P, Švajdler M, Agaimy A, Hadravský L, Kalmykova AV, Konishi E, Heidenreich...
Thu Jul 30, 2020 13:01
Related Articles Chest Wall Implantation Metastasis Caused by Percutaneous Interventional Procedure Appearing 12 Years After Liver Transplantation: A Case Report. Transplant Proc. 2020 Mar;52(2):587-588 Authors: López Ortega S, González Grande R, Santaella Leiva I, De la Cruz Lombardo J, Jiménez Pérez M Abstract Percutaneous treatments (mainly radiofrequency ablation and ethanol injection) are modes of treatment for hepatocellular carcinoma....
Thu Jul 30, 2020 13:01
Related Articles The clinicopathological spectrum of pseudomyogenic hemangioendothelioma: report of an additional series with review of the literature. Virchows Arch. 2020 Aug;477(2):231-240 Authors: Sun Y, Zhao M, Lao IW, Yu L, Wang J Abstract We present here our experience with 24 cases of pseudomyogenic hemangioendothelioma (PMHE) to further delineate its clinicopathological spectrum. There were 18 males and 6 females with a median age of...
Thu Jul 30, 2020 13:01
Related Articles Tumor budding is an adverse prognostic marker in intestinal-type sinonasal adenocarcinoma and seems to be unrelated to epithelial-mesenchymal transition. Virchows Arch. 2020 Aug;477(2):241-248 Authors: Maffeis V, Cappellesso R, Galuppini F, Guzzardo V, Zanon A, Cazzador D, Emanuelli E, Ventura L, Martini A, Fassina A Abstract Intestinal-type adenocarcinoma (ITAC) of sinonasal tract is a rare malignant tumor with strong morphological,...
Thu Jul 30, 2020 13:01
Related Articles Relevance of routine pathology review in cervical carcinoma. Virchows Arch. 2020 Aug;477(2):301-307 Authors: van Beekhuizen HJ, Freulings MD, Dasgupta S, van Kemenade FJ, Ewing-Graham PC, van Doorn HC Abstract To determine the impact of pathology review on the management of patients with cervical carcinoma, 264 reports of pathology review from 230 patients referred to Erasmus MC (2010-2012) were studied retrospectively. Discrepancies...
Thu Jul 30, 2020 13:01
Related Articles Alveolar Rhabdomyosarcoma Following Mandibular Distraction Osteogenesis. J Craniofac Surg. 2020 May/Jun;31(3):e256-e258 Authors: Hassan B, Jacob DD, Sisti A, Zahler S, Rampazzo A, Bassiri Gharb B Abstract The authors present a rare case of anaplastic alveolar rhabdomyosarcoma (ARMS) occurring after Mandibular Distraction Osteogenesis. A 16-month-old male presented with a rapidly enlarging left lower jaw mass after removal of...
Thu Jul 30, 2020 13:01
Related Articles Bing-Neel syndrome presenting as isolated CNS lymphoplasmacytic lymphoma: A case report and review of the literature. J Clin Neurosci. 2020 Jan;71:277-280 Authors: Grainger BT, Issa S Abstract Bing-Neel syndrome (BNS) is characterised by infiltration of the central nervous system by lymphoplasmacytic lymphoma (LPL) cells and is traditionally regarded as a complication of pre-existing systemic Waldenström's macroglobulinaemia...
Thu Jul 30, 2020 13:01
Related Articles Mismatch Repair Protein Deficiency/Microsatellite Instability Is Rare in Cholangiocarcinomas and Associated With Distinctive Morphologies. Am J Clin Pathol. 2020 04 15;153(5):598-604 Authors: Ju JY, Dibbern ME, Mahadevan MS, Fan J, Kunk PR, Stelow EB Abstract OBJECTIVES: Although germline mutations of mismatch repair (MMR) genes (Lynch syndrome) are not typically associated with cholangiocarcinomas, the US Food and Drug Administration...
Thu Jul 30, 2020 13:01
Related Articles Successful resolution of the ophthalmic manifestations of a falcotentorial meningioma through Cerebrospinal fluid diversion. J Clin Neurosci. 2020 Jan;71:281-283 Authors: Pham C, McAlpine H, Tee JW Abstract We report the case of a falcotentorial meningioma presenting only with binocular, horizontal diplopia in an otherwise healthy sixty-two-year old male. Review of the established literature highlights a lack of consensus regarding...
Thu Jul 30, 2020 13:01
Related Articles Epstein-Barr virus-associated T- and NK-cell lymphoproliferative diseases: an update and diagnostic approach. Pathology. 2020 Jan;52(1):111-127 Authors: Hue SS, Oon ML, Wang S, Tan SY, Ng SB Abstract Epstein-Barr virus (EBV)-positive T-cell and natural killer (NK)-cell lymphoproliferative diseases (EBV-TNKLPD) are a group of uncommon disorders characterised by EBV infection of T- and NK-cells. As a group, EBV-TNKLPD are more...
Thu Jul 30, 2020 13:01
Related Articles Rhabdomyomatous mesenchymal hamartoma developed at an unexpected location. Arch Argent Pediatr. 2019 10 01;117(5):e519-e522 Authors: Sayan A, Diniz G, Mert M, Yildirim Ekin Z, Koyluoglu G Abstract Rhabdomyomatous mesenchymal hamartoma is a rare dermal lesion which was first described in 1986 as "striated muscle hamartoma". It usually develops in the head and neck region of newborns. We report a 38-day-old girl with a congenital...
Thu Jul 30, 2020 13:01
Related Articles [Vogt-Koyanagi-Harada-like uveitis under immune checkpoint inhibitor treatment for metastasized malignant melanoma]. Ophthalmologe. 2020 May;117(5):467-471 Authors: Mihailovic N, Dyballa J, Herz S, Fluck M, Alnawaiseh M, Merté RL, Eter N Abstract This article presents the case of a 68-year-old female patient who reported bilateral progressive visual loss over 4 weeks. The patient had a known metastatic malignant cutaneous melanoma,...
Thu Jul 30, 2020 13:01
Related Articles Prevalence of genetic susceptibility for breast and ovarian cancer in a non-cancer related study population: secondary germline findings from a Swiss single centre cohort. Swiss Med Wkly. 2019 Aug 12;149:w20092 Authors: Kraemer D, Azzarello-Burri S, Steindl K, Boonsawat P, Zweier M, Dedes KJ, Joset P, Fink D, Rauch A Abstract BACKGROUND: Since the advent of high-throughput sequencing technologies, organised germline screening,...
Thu Jul 30, 2020 13:01
Related Articles Fibrocartilaginous Embolism of the Spinal Cord in Children: A Case Report and Review of Literature. Pediatr Neurol. 2019 10;99:3-6 Authors: Yamaguchi H, Nagase H, Nishiyama M, Tokumoto S, Toyoshima D, Akasaka Y, Maruyama A, Iijima K Abstract Fibrocartilaginous embolism is assumed to be caused by fibrocartilaginous nucleus pulposus component migration through retrograde embolization to the spinal cord artery. Fibrocartilaginous...
Thu Jul 30, 2020 13:01
Related Articles Diagnosing synovial sarcoma by fine-needle aspiration cytology and molecular techniques. Cytopathology. 2019 09;30(5):504-509 Authors: Zhang Y, Wessman S, Wejde J, Tani E, Haglund F Abstract OBJECTIVE: Synovial sarcomas (SS) are rare soft tissue tumours defined by the SYT-SSX fusion gene. The tumours are composed of mesenchymal cells with varying degrees of epithelial differentiation. Cytomorphological descriptive studies are...
Thu Jul 30, 2020 13:01
Related Articles Orbital AL amyloid. Orbit. 2020 Feb;39(1):68-70 Authors: Chan TM, Prospero Ponce CM, Allen RC, Bell D, Lee AG Abstract Amyloidosis and lymphoma localized to the ocular adnexa are rare, and their presentation may resemble more common inflammatory conditions such as autoimmune disease or infection, which can protract diagnostic evaluation and delay eventual therapy. In a patient with recalcitrant facial and tooth pain and ophthalmoplegia,...
Thu Jul 30, 2020 13:01
Related Articles Pancreatic acinar cell carcinoma is associated with BRCA2 germline mutations: a case report and literature review. Cancer Biol Ther. 2019;20(7):949-955 Authors: Kryklyva V, Haj Mohammad N, Morsink FHM, Ligtenberg MJL, Offerhaus GJA, Nagtegaal ID, de Leng WWJ, Brosens LAA Abstract Acinar cell carcinoma (ACC) is a rare pancreatic neoplasm with dismal prognosis. Insights into the molecular basis of ACC can pave the way for the...
Thu Jul 30, 2020 13:01
Related Articles Fibromatosis colli: A rare cause of neck mass with cytological soft pointers. Cytopathology. 2019 09;30(5):549-551 Authors: Kumar P, Sharma S, Kapil V PMID: 30869804 [PubMed - indexed for MEDLINE]
Thu Jul 30, 2020 13:01
Related Articles Soft-Tissue Metastases From Esophageal Cancer. J Gastrointest Surg. 2019 09;23(9):1721-1728 Authors: El Abiad JM, Hales RK, Levin AS, Morris CD Abstract BACKGROUND: Metastatic carcinoma to skeletal muscle and/or subcutaneous fat is a rare event. Only 27 cases of esophageal cancer to soft tissue have been described in the English-language literature. PURPOSE: Our goal was to describe the prevalence and clinical characteristics...
Thu Jul 30, 2020 13:01
Related Articles Pseudocystic appearance of an orbital carcinoid metastasis. Orbit. 2020 Feb;39(1):41-44 Authors: Halliday LA, Curragh D, Sia PI, Selva D Abstract Carcinoid tumours are a low-grade neuroendocrine malignancy that infrequently metastisizes to orbital structures. The typical radiological appearance of carcinoid is a solid, well-circumscribed mass that enhances with contrast. We present a case of orbital carcinoid metastasis with...
Thu Jul 30, 2020 13:01
Related Articles Comprehensive three-dimensional morphology of neoangiogenesis in pulmonary veno-occlusive disease and pulmonary capillary hemangiomatosis. J Pathol Clin Res. 2019 04;5(2):108-114 Authors: Neubert L, Borchert P, Shin HO, Linz F, Wagner WL, Warnecke G, Laenger F, Haverich A, Stark H, Hoeper MM, Kuehnel M, Ackermann M, Jonigk D Abstract Pulmonary veno-occlusive disease (PVOD) is a rare lung disease characterized by fibrotic narrowing...
Thu Jul 30, 2020 13:01
Related Articles Delayed Occipitocervical Instability With Cranial Settling After Far-Lateral Transcondylar Surgery for Invasive Skull Base Tumor. Oper Neurosurg (Hagerstown). 2019 02 01;16(2):250-255 Authors: Mazur MD, Dailey AT, Shah L, Scoville JP, Couldwell WT Abstract BACKGROUND: Occipitocervical instability is a rare but potentially severe complication of a far-lateral transcondylar surgical approach to the skull base. OBJECTIVE:...
Thu Jul 30, 2020 13:01
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