Related Articles[A case of rare laryngeal neurogenic tumor]. Wiad Lek. 2019;72(7):1413-1414 Authors: Czubak J, Frączek M, Morawski K Abstract Laryngeal schwannoma is a rare benign tumour of the larynx. Schwannomas derive from the Schwann cells. Magnetic resonance imaging (MRI) is the best imaging tool for suggesting the diagnosis. We report case of laryngeal schwannoma. The case was a 61-year-old man with a 1-year history of dysphonia and stridor. Laryngoscopy...
Related Articles[A Case of Small Cell Lung Cancer Diagnosed with Metastasis-Induced Acute Pancreatitis]. Gan To Kagaku Ryoho. 2019 Jul;46(7):1175-1177 Authors: Ito N, Oshita H, Isoyama S, Senoo M, Kawasaki K, Okusaki K Abstract A 56-year-old man was admitted to our hospital for management of acute epigastric abdominal pain and elevation of pancreatic enzymes. The CT scan revealed enlargement ofthe pancreatic body as well as the lung tumor ofthe right...
Related Articles[A Case of Duodenal Perforation during Bevacizumab Combination Chemotherapy in a Patient with Multiple Lung Metastasis after a Sigmoidectomy]. Gan To Kagaku Ryoho. 2019 May;46(5):953-955 Authors: Suzumura H, Shinozaki H, Kondo R, Yamaguchi M, Torizaki Y, Ozawa Y, Futoh Y, Matsuoka T, Matsumoto K, Inoue M, Sasakura Y, Terauchi T, Kimata M, Furukawa J, Kobayashi K, Ogata Y Abstract A 73-year-old man underwent laparoscopic sigmoidectomy...
Related Articles[Successful Treatment of T-Cell Prolymphocytic Leukemia with Alemtuzumab]. Gan To Kagaku Ryoho. 2019 May;46(5):913-915 Authors: Ueki D, Yoshida C, Tsutsumi Oota I, Seki M, Komeno T, Ito H, Ide Y Abstract T-cell prolymphocytic leukemia(T-PLL)is a highly aggressive hematopoietic malignancy with poor prognosis and is extremely rare in Japan. Since T-PLL cells usually express high levels of CD52, the anti-CD52 monoclonal antibody alemtuzumab...
Related Articles[A Case of Myeloid Sarcoma That Primarily Developed in the Spleen]. Gan To Kagaku Ryoho. 2019 Apr;46(4):784-786 Authors: Kado T, Tanemura M, Furukawa K, Mikamori M, Saito T, Ohtsuka M, Suzuki Y, Imasato M, Kishi K, Akamatsu H Abstract We report a case of myeloid sarcoma(MS)that primarily developed in the spleen. The patient was a 60s man with a chief complainant of low-grade fever following a dental implant. Although he underwent intensive...
Related Articles[A Rare Case of Adenosquamous Carcinoma in the Liver with Hepatolithiasis]. Gan To Kagaku Ryoho. 2019 Apr;46(4):772-774 Authors: Harino T, Tomimaru Y, Noguchi K, Nagase H, Ogino T, Hirota M, Oshima K, Tanida T, Noura S, Imamura H, Akagi K, Iwazawa T, Tamura H, Adachi S, Dono K Abstract This report describes a case of primary adenosquamous carcinoma of the liver with hepatolithiasis. A 70's man was followed up at a clinic for hepatolithiasis,...
Related Articles[A Case of Leiomyosarcoma of the Sigmoidal Mesocolon]. Gan To Kagaku Ryoho. 2019 Apr;46(4):769-771 Authors: Takase K, Murata K, Naito A, Mori R, Nose Y, Kawai K, Sakamoto T, Murakami K, Katsura Y, Omura Y, Masuzawa T, Kagawa Y, Takeno A, Takeda Y Abstract Leiomyosarcoma of the mesocolon is a very rare disease. Previously, there was no recommendation for chemotherapy or radiotherapy for leiomyosarcoma of the mesocolon, and only surgical...
Related Articles[A Case of Rectal Neuroendocrine Carcinoma That Developed Two Years after Curative Resection for Sigmoid Colon Cancer]. Gan To Kagaku Ryoho. 2019 Apr;46(4):727-729 Authors: Fujimoto T, Konno S, Usuda A, Yagawa Y, Yokomizo H, Matsumoto A, Yano Y, Okayama S, Satake M, Yamada Y, Yoshimatsu K, Naritaka Y Abstract We report a rare case ofrectal neuroendocrine carcinoma(NEC)following sigmoidectomy of sigmoid colon cancer. NEC of the rectum...
Related Articles[A Case of Recurrent Small Bowel Cancer That Successfully Responded to Chemoradiation Therapy]. Gan To Kagaku Ryoho. 2019 Apr;46(4):705-708 Authors: Murakami D, Matsuda K, Yokoyama S, Tamura K, Iwamoto H, Mizumoto Y, Deguchi M, Nakamura Y, Yamaue H Abstract Primary small bowel cancer is a rare entity; thus, it is often found in progress. Therefore, the prognosis is often poor. Because of its low frequency, there are few reports concerning...
Related ArticlesElectrical Remodeling of Ventricular Repolarization Abnormality after Treatment in Pheochromocytoma: U Wave Finding in a Retrospective Analysis. Biomed Res Int. 2019;2019:2605323 Authors: Stolfo GD, Mastroianno S, Maggio A, De Luca G, Potenza DR, Salvatori MP, Russo A Abstract Background: Pheochromocytoma is a rare neuroendocrine tumor, clinically characterized by high blood pressure, palpitations, and headache. It is often associated...
Related ArticlesThe Importance of Data Compression in the Field of Genomics. IEEE Pulse. 2019 Mar-Apr;10(2):20-23 Authors: Greenfield D, Wittorff V, Hultner M Abstract Genomic research is the driver of efforts to create personalized medicine and discover cures for cancer, rare diseases, and other serious health conditions. Thanks to the widespread availability of inexpensive genome sequencing technology, the field is expanding rapidly. Many countries...
Related ArticlesSpectrum of mutations in the RB1 gene in Vietnamese patients with retinoblastoma. Mol Vis. 2019;25:215-221 Authors: Kiet NC, Khuong LT, Minh DD, Nguyen The Vinh, Quan NHM, Xinh PT, Trang NNC, Luan NT, Khai NM, Vu HA Abstract Purpose: Retinoblastoma (RB) is a rare childhood malignant disorder caused by the biallelic inactivation of the RB1 gene. Early diagnosis and identification of carriers of heritable mutations in RB1 can improve disease...
Related ArticlesA case for consideration by apheresis practitioners: Melanoma and PD-1 inhibitor treatment in a patient with multiple relapses of immune thrombotic thrombocytopenic purpura. Transfus Apher Sci. 2019 Apr;58(2):123-124 Authors: Nicholson MC, Pavenski K, Trinkaus M Abstract Thrombotic Thrombocytopenic Purpura (TTP) is a rare life-threatening disease caused by ADAMTS-13 deficiency. Up to forty percent of patients with TTP relapse, and most...
Related ArticlesRefractory Thrombotic Thrombocytopenic Purpura in a patient with Kaposi sarcoma. Transfus Apher Sci. 2019 Apr;58(2):187-189 Authors: Sahin O, Albayrak M, Yıldız A, Pala Ç, Aktas L, Maral S, Afacan Öztürk HB, Cömert P Abstract The case is here presented of a 70-year old male patient with rare coexistence of Kaposi Sarcoma and resistant Thrombotic Thrombocytopenic Purpura (TTP). The Kaposi lesions were determined before the diagnosis of...
Related ArticlesIndocyanine Green Sentinel Node in Merkel Cell Carcinoma of the Cheek. J Craniofac Surg. 2019 Jun;30(4):e376-e377 Authors: Gabriele G, Aboh IV, Cascino F, Zerini F, Amadi JU, Del Frate R, Xu J, Gennaro P Abstract Merkel cell carcinoma (MCC) is a rare malignant tumor with a neuroendocrine phenotype. The authors report a case of MCC of the left cheek region in an 85-year-old Caucasian woman who also received sentinel node biopsy using...
Related ArticlesCytologic diagnosis of metastatic malignant phyllodes tumor of the breast in pleural effusion. Diagn Cytopathol. 2019 Jun;47(6):599-602 Authors: Li JJX, Chan WC, Chau HHL, Wu C, Tse GM Abstract A 54-year-old woman presented with a left breast mass, discovered 4 years ago but was static until 2 months before presentation, when it showed a rapid increase in size and became painful. Mammography showed a large lobulated mass with internal...
Related ArticlesFine-needle aspiration cytology of metastatic spindle cell follicular thyroid carcinoma: A case report. Diagn Cytopathol. 2019 Jun;47(6):608-611 Authors: Chen YH, Perrino CM, Cheng L, Wu HH Abstract Follicular thyroid carcinoma, spindle cell variant is extremely rare. The tumor is predominantly composed of spindle cells with a fusiform appearance that are arranged in intersecting fascicles. Fine-needle aspiration biopsy of this entity...
Related ArticlesMidline carcinoma expressing NUT in malignant effusion cytology. Diagn Cytopathol. 2019 Jun;47(6):594-598 Authors: Shenoy KD, Stanzione N, Caron JE, Fishbein GA, Abtin F, Lluri G, Hirschowitz SL Abstract Nuclear protein in testis (NUT) midline carcinoma (NMC) is a rare and aggressive subset of poorly differentiated squamous cell carcinoma that is defined by t(15,19) and typically presents in the midline structures of the head, neck,...
Related ArticlesCytological features of uterine carcinosarcoma: A retrospective study of 20 cases with an emphasis on the usefulness of endometrial cytology. Diagn Cytopathol. 2019 Jun;47(6):547-552 Authors: Okano K, Ishida M, Sandoh K, Mizokami T, Kita M, Okada H, Tsuta K Abstract BACKGROUND: Carcinosarcoma of the endometrium is a relatively rare but aggressive neoplasm. Endometrial cytological features of this type of tumor have been rarely reported....
Related ArticlesSclerosing mucoepidermoid carcinoma with eosinophilia of the thyroid: Case report of a rare lesion with novel genetic mutation. Diagn Cytopathol. 2019 Jun;47(6):589-593 Authors: Wiles AB, Kraft AO, Mueller SM, Powers CN Abstract Sclerosing mucoepidermoid carcinoma with eosinophilia (SMECE) is a rare primary cancer of the thyroid. This tumor is analogous to other primary tumors of the salivary glands, breast, pancreas, and esophagus....
Related ArticlesOncocytic poorly differentiated (insular) thyroid carcinoma mimicking metastatic adenocarcinoma. A case report and review of the literature. Diagn Cytopathol. 2019 Jun;47(6):584-588 Authors: Laforga JB, Cortés VA Abstract We report the cytohistologic and immunohistochemical findings of an oncocytic variant of poorly differentiated thyroid carcinoma in a 76-year old man with a prior history of prostatic adenocarcinoma. The man complained...
Related ArticlesCastleman's disease: A rare cause of an axillary mass mimicking breast metastasis. Breast J. 2019 01;25(1):147-148 Authors: Barna B, Sabri S, Chitnis A, Arora P, Hunt R PMID: 30592111 [PubMed - indexed for MEDLINE]
Related ArticlesAntracosilicosis: A Rare Cause of Endobronchial "Tumor". J Bronchology Interv Pulmonol. 2019 Jan;26(1):e5-e7 Authors: Cullivan S, Murphy DM, Kennedy MP PMID: 30562284 [PubMed - indexed for MEDLINE]
Related ArticlesIntramuscular lipoma originating in pectoralis major: A rare presentation of a large breast mass. Breast J. 2019 01;25(1):145-146 Authors: Dubyk F, Maqbool B, Gill AA, Fine S PMID: 30488585 [PubMed - indexed for MEDLINE]
Related ArticlesMultimodality Imaging of a Rare Atrioventricular Nodal Tumor. Circ Cardiovasc Imaging. 2018 10;11(10):e008159 Authors: Fiset S, Butany J, Ing DJ, Cusimano RJ, Nguyen ET PMID: 30354481 [PubMed - indexed for MEDLINE]
Related ArticlesRight Temporal Brain Metastases Arising Three Years after Curative Resection of Gastric Cancer: A Case Report. Gulf J Oncolog. 2018 Sep;1(28):75-77 Authors: Azzam AZ, Dababo MA, Azzam KA, Almeshal M, Amin TM Abstract BACKGROUND: Gastric cancer can metastasize to multiple organs but the metastases to brain is very rare. We report a case of recurrent gastric cancer. The only site of recurrence is brain metastases that occurred three years...
Related ArticlesClinicopathological outcome of ovarian granulosa cell tumors. Gulf J Oncolog. 2018 Sep;1(28):31-36 Authors: Al-Rayyan E, Maaita M, Alelwan O, Taso O, Hadadin W Abstract OBJECTIVE: The aim of our study was to analyze the clinical and pathological characteristics of women who were diagnosed with malignant ovarian granulosa cell tumors and managed at single institution. MATERIALS AND METHODS: A retrospective study was conducted...
Related ArticlesCutaneous inflammation as a marker of malignant transformation in a patient with linear unilateral basaloid follicular hamartoma. Indian J Dermatol Venereol Leprol. 2019 May-Jun;85(3):287-290 Authors: Del Barrio-Diaz P, Meza-Romero R, González S, Vera-Kellet C Abstract Basaloid follicular hamartoma is a rare, benign and superficial malformation of hair follicles, characterized histologically by epithelial proliferation of basaloid cells...
Related ArticlesDiverse EGFR Exon 20 Insertions and Co-Occurring Molecular Alterations Identified by Comprehensive Genomic Profiling of NSCLC. J Thorac Oncol. 2018 10;13(10):1560-1568 Authors: Riess JW, Gandara DR, Frampton GM, Madison R, Peled N, Bufill JA, Dy GK, Ou SI, Stephens PJ, McPherson JD, Lara PN, Burich RA, Ross JS, Miller VA, Ali SM, Mack PC, Schrock AB Abstract INTRODUCTION: EGFR exon 20 insertions (EGFRex20ins) comprise an uncommon subset...
Related ArticlesRare Variants in Known Susceptibility Loci and Their Contribution to Risk of Lung Cancer. J Thorac Oncol. 2018 10;13(10):1483-1495 Authors: Liu Y, Lusk CM, Cho MH, Silverman EK, Qiao D, Zhang R, Scheurer ME, Kheradmand F, Wheeler DA, Tsavachidis S, Armstrong G, Zhu D, Wistuba II, Chow CB, Behrens C, Pikielny CW, Neslund-Dudas C, Pinney SM, Anderson M, Kupert E, Bailey-Wilson J, Gaba C, Mandal D, You M, de Andrade M, Yang P, Field JK, Liloglou T, Davies...
Related Articles[Squamous cell carcinoma of the nasal vestibule - Review of literature]. Laryngorhinootologie. 2018 06;97(6):379-391 Authors: Koopmann M, Rudack C, Weiss D, Stenner M Abstract BACKGROUND: Squamous cell carcinoma of the nasal vestibule is a rare entity. In consequence disagreement in etiology, staging system and therapy of primary tumor with or without adjuvant treatment of regional lymph nodes are apparent. METHODS: Pubmed-Recherche...
Related ArticlesA Rare Large Symptomatic Paratracheal Air Cyst in a 62-Year-Old Woman. Ann Thorac Surg. 2018 12;106(6):e305-e307 Authors: Arian Nia A, Ghelichli M, Bakhshi T, Vahidirad A Abstract Paratracheal air cysts are lesions adjacent to trachea. They are often asymptomatic and are found usually as an incidental finding in imaging. The pathology of these lesions is unclear and they can be congenital or acquired. Paratracheal air cysts rarely cause...
Related ArticlesAn In Vivo Screen Identifies PYGO2 as a Driver for Metastatic Prostate Cancer. Cancer Res. 2018 07 15;78(14):3823-3833 Authors: Lu X, Pan X, Wu CJ, Zhao D, Feng S, Zang Y, Lee R, Khadka S, Amin SB, Jin EJ, Shang X, Deng P, Luo Y, Morgenlander WR, Weinrich J, Lu X, Jiang S, Chang Q, Navone NM, Troncoso P, DePinho RA, Wang YA Abstract Advanced prostate cancer displays conspicuous chromosomal instability and rampant copy number aberrations,...
Related ArticlesClinical Outcome and Molecular Analysis of a Chinese Patient With Lung Adenocarcinoma Harboring Rare EGFR Mutation V834L. J Thorac Oncol. 2018 10;13(10):e189-e191 Authors: Li J, Zhang L, Wu Y, Yang W, Yang Z, Zhang H PMID: 29705137 [PubMed - indexed for MEDLINE]
Related ArticlesAlloHSCT for inv(3)(q21;q26)/t(3;3)(q21;q26) AML: a report from the acute leukemia working party of the European society for blood and marrow transplantation. Bone Marrow Transplant. 2018 06;53(6):683-691 Authors: Halaburda K, Labopin M, Houhou M, Niederwieser D, Finke J, Volin L, Maertens J, Cornelissen JJ, Milpied N, Stuhler G, Kröger N, Esteve J, Mohty M, Nagler A Abstract Acute myeloid leukemia with inv(3)(q21;q26.2)/t(3;3)(q21;q26.2)...
Related ArticlesSynovial sarcoma complicating Maffucci syndrome. Indian J Dermatol Venereol Leprol. 2019 May-Jun;85(3):291-294 Authors: Gammoudi R, Aounallah A, Belajouza C, Nouira R Abstract Maffucci syndrome is a rare nonhereditary disorder comprising of lymphovascular malformations and multiple enchondromas, which may be associated with several internal malignancies. This report describes a new association of Maffucci syndrome with pedal synovial...
Related ArticlesCollaborating with our adult colleagues: A case series of robotic surgery for suspicious and cancerous lesions in children and young adults performed in a free-standing children's hospital. J Pediatr Urol. 2018 04;14(2):182.e1-182.e8 Authors: Varda BK, Cho P, Wagner AA, Lee RS Abstract BACKGROUND: In adult urologic oncology the use of robotics has become commonplace; in pediatric urology it is rare. Herein, we describe a collaboration...
Related ArticlesEvaluating Treatment Patterns for Small Cell Carcinoma of the Colon Using the National Cancer Database (NCDB). J Gastrointest Cancer. 2019 Jun;50(2):244-253 Authors: Balasubramanyam S, O'Donnell BP, Musher BL, Jhaveri PM, Ludwig MS Abstract OBJECTIVE(S): The objective of this study was to characterize the clinicopathological prognostic factors and treatment patterns for small cell carcinoma (SCC) of the colon, a rare disease without standard...
Related ArticlesMosaic NRASopathy n a child with giant melanocytic congenital naevus, epidermal hamartoma and bilateral nephroblastomatosis: clinical implication for follow-up. J Eur Acad Dermatol Venereol. 2018 Jul;32(7):e258-e260 Authors: Maridet C, Morice-Picard F, Gros A, Crivelli L, de la Fouchardière A, Vergier B, Taïeb A PMID: 29314428 [PubMed - indexed for MEDLINE]
Related ArticlesHepatocellular carcinoma in a free-living marmoset (Callithrix sp.) with concomitant biliary trematodiasis. J Med Primatol. 2018 04;47(2):128-131 Authors: Díaz-Delgado J, Sanches TC, Dos Santos-Cirqueira C, Coimbra AAC, Guerra JM, Joppert A, Di Loretto C, Rizardi MB, Sansone M, Nagamori FO, Gonçalves PS, Ressio R, Iglezias S, Fernandes NCCA, Kanamura C, Groch KR, Catão-Dias JL Abstract Hepatocellular carcinoma (HCC) is rare in New World...
Related ArticlesPatterns of lymph node sampling and the impact of lymph node density in favorable histology Wilms tumor: An analysis of the national cancer database. J Pediatr Urol. 2018 04;14(2):161.e1-161.e8 Authors: Saltzman AF, Carrasco A, Amini A, Aldrink JH, Dasgupta R, Gow KW, Glick RD, Ehrlich PF, Cost NG Abstract INTRODUCTION: There is controversy about the role of lymph node (LN) sampling or dissection in the management of favorable histology...
Related ArticlesAcute simultaneous development of brain tumour-like lesion and demyelinating polyneuropathy in a patient with chronic relapsing myelitis. Mult Scler. 2018 04;24(4):546-550 Authors: Puthenparampil M, Terrin A, Federle L, Gizzi M, Perini P, Gallo P Abstract Combined central and peripheral demyelination (CCPD) is a rare chronic inflammatory disorder of the nervous system. We describe the case of a patient with a history of recurrent myelitis...
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