Related ArticlesSialolipoma of Parotid Gland a Rare Histological Presentation. Indian J Otolaryngol Head Neck Surg. 2019 Oct;71(Suppl 1):805-808 Authors: Shrikrishna BH, Patel VI, Stephan R, Mazhar MS Abstract Sialolipoma is a rare tumour found within both major and minor salivary glands, it is recently described as a variant of salivary gland lipoma. Sialolipoma was first described by Pusiol et al. (Indian J Pathol Microbiol 52(3):379-382, 2009). Sialolipoma...
Wed Nov 20, 2019 14:38
Related ArticlesSolitary Fibrous Tumor of the Dorsal Tongue Area. Indian J Otolaryngol Head Neck Surg. 2019 Oct;71(Suppl 1):759-761 Authors: Vuckovic NM, Vuckovic DC, Ilic MP, Mijatov SM Abstract Solitary fibrous tumor (SFT) is a rare tumor occurring in pleura or extrapleural areas. The tongue is infrequently affected, in less than 25 published cases. A female patient, 35 years of age, noticed an oval mass in the posterior dorsal part of the tongue....
Wed Nov 20, 2019 14:38
Related ArticlesA Rare Case of Locally Advanced Recurrent Neuroendocrine Tumour of Neck Salvaged by a Radical Surgical Approach. Indian J Otolaryngol Head Neck Surg. 2019 Oct;71(Suppl 1):74-78 Authors: Sundaram SS, Robbins S, Priya D Abstract Neuroendocrine tumours of head and neck are rare neoplasms and even more rare are those of cutaneous adenoid cystic carcinoma with neuroendocrine differentiation. Virtually every known variant of neoplasia with...
Wed Nov 20, 2019 14:38
Related ArticlesSystematic mutation analysis in rare colorectal cancer presenting ovarian metastases. Sci Rep. 2019 Nov 18;9(1):16990 Authors: Park S, Ahn HK, Lee DH, Jung Y, Jeong JW, Nam S, Lee WS Abstract Although colorectal cancer is one of the most lethal cancer types in the world, its metastasis to the ovary is rare, compared to metastasis to other organs. Consequently, the genomic basis for colon-to-ovary metastasis remains unstudied, due to limited...
Wed Nov 20, 2019 13:07
Related ArticlesBone Sarcomas and Desmoids. Hematol Oncol Clin North Am. 2020 Feb;34(1):177-188 Authors: Brownstein JM, DeLaney TF Abstract Bone sarcomas are rare tumors arising in bone, representing only a small fraction of solid malignant tumors. Desmoids are benign, infiltrative soft tissue neoplasms. Because of their scarcity and a paucity of data, the management of these tumors can be challenging, especially for clinicians who infrequently encounter...
Wed Nov 20, 2019 13:07
Related Articles[A Case of Dedifferentiated Liposarcoma of the Spermatic Cord]. Hinyokika Kiyo. 2019 Oct;65(10):429-434 Authors: Tobiume M, Aoki S, Yamada Y, Hara K, Muramatsu H, Nishikawa G, Ono K, Nakamura K Abstract Liposarcomas are most commonly found in the extremities, in the retroperitoneum and, less often, in the head and neck area. The spermatic cord is a rare site of origin, accounting for about 4-7% of all liposarcomas. We report a case of...
Wed Nov 20, 2019 13:07
Related Articles[Clinical Effect of Nivolumab on Advanced Renal Cell Carcinoma with Peritoneal Metastasis]. Hinyokika Kiyo. 2019 Oct;65(10):413-419 Authors: Hida T, Yamasaki T, Banno H, Fuchigami Y, Hattahara K, Fujiwara M, Suzuki R, Kita Y, Yoshino T, Goto T, Sawada A, Akamatsu S, Saito R, Kobayashi T, Inoue T, Ogawa O Abstract Peritoneal dissemination or metastasis is a relatively rare presentation of renal cell carcinoma. We report four cases of advanced...
Wed Nov 20, 2019 13:07
Related Articles[METASTATIC Mucinous Tubular and Spindle Cell Carcinoma Treated with Nivolumab Successfully : A Case Report]. Hinyokika Kiyo. 2019 Sep;65(9):363-367 Authors: Takahashi Y, Numakura K, Aoyama Y, Okada S, Saito T, Muto Y, Koizumi A, Nara T, Chiba S, Kanda S, Saito M, Narita S, Inoue T, Satoh S, Nanjo H, Habuchi T Abstract A 68-year-old man was referred to our hospital with a right-sided renal tumor identified by ultrasonography at the time...
Wed Nov 20, 2019 13:07
Related Articles[Epidemioclinical and ultrasonographic profile of hydatidiform moles in Abidjan]. Pan Afr Med J. 2019;33:264 Authors: N'goran K, Eric KK, Brahima D, Alihonou S, Nicaise KA, Jean-Jacques EK, Anne-Marie ND, Victorien KA Abstract Introduction: The purpose of our study was to describe the epidemioclinical and ultrasonographic features of hydatidiform moles (HM) in Abidjan. Methods: We conducted a cross-sectional study in the Department...
Wed Nov 20, 2019 13:07
Related ArticlesParatesticular liposarcoma: a case report. Pan Afr Med J. 2019;33:282 Authors: Mouden K, Wakrim S, Semmar A Abstract Paratesticular liposarcomas (PLS) is a very uncommon pathology type of paratesticular sarcomas, with less 200 similar cases reported to date in the English literature. There are a few cases regarding giant paratesticular liposarcoma measuring over 10 cm. We present an unusual case with a giant well differentiated PLS...
Wed Nov 20, 2019 13:07
Related Articles[Cyst of the broken common bile duct: literature review]. Pan Afr Med J. 2019;33:276 Authors: Azahouani A, Zaari N, Aissaoui FE, Hida M, Fitri M, Benradi L, Benhaddou H Abstract Cystic malformations of the bile ducts are rare congenital disorders, with an incidence of 1/2000000 live births. Complication including the angiocholitis, chronic pancreatitis, progressive biliary cirrhosis, portal hypertension or gallbladder lithiases can...
Wed Nov 20, 2019 13:07
Related Articles[Paraneoplastic neurologic degeneration revealing ovarian cancer recurrence]. Pan Afr Med J. 2019;33:281 Authors: Zouiten O, Benbrahim Z, Amaadour L, Mellas N Abstract Paraneoplastic neurologic degeneration (PND) is characterized by acute and subacute onset neurological syndrome associated with active or with subclinical cancer. It is rare but early diagnosis can improve the neurological and carcinological prognosis. Among the PNDs...
Wed Nov 20, 2019 13:07
Related Articles[Occipital condyle syndrome: the visible part of the iceberg]. Pan Afr Med J. 2019;33:268 Authors: Raggabi A, Lalya I, Bourazza A Abstract Occipital condyle syndrome is a rare clinical disorder, clinically defined by the association of intense occipital headaches and paralysis of the twelfth paired cranial nerve. Its etiology is dominated by metastatic tumor. Imaging is the gold standard for diagnosis allowing to highlight occipital...
Wed Nov 20, 2019 13:07
Related ArticlesSomatic mutations and clonal dynamics in healthy and cirrhotic human liver. Nature. 2019 10;574(7779):538-542 Authors: Brunner SF, Roberts ND, Wylie LA, Moore L, Aitken SJ, Davies SE, Sanders MA, Ellis P, Alder C, Hooks Y, Abascal F, Stratton MR, Martincorena I, Hoare M, Campbell PJ Abstract The most common causes of chronic liver disease are excess alcohol intake, viral hepatitis and non-alcoholic fatty liver disease, with the clinical...
Wed Nov 20, 2019 13:07
Related ArticlesDifficulties in the diagnosis of periapical translucencies and in the classification of cemento-osseous dysplasia. BMC Oral Health. 2019 07 10;19(1):139 Authors: Brody A, Zalatnai A, Csomo K, Belik A, Dobo-Nagy C Abstract BACKGROUND: Cemento-osseous dysplasia is a benign fibro-osseous lesion of the tooth-bearing region of the jaws with a periodontal ligament origin. It appears predominantly in Black and Asian middle-aged females. Its...
Wed Nov 20, 2019 13:07
Related ArticlesFactors influencing malignant mesothelioma survival: a retrospective review of the National Mesothelioma Virtual Bank cohort. F1000Res. 2018;7:1184 Authors: Amin W, Linkov F, Landsittel DP, Silverstein JC, Bashara W, Gaudioso C, Feldman MD, Pass HI, Melamed J, Friedberg JS, Becich MJ Abstract Background: Malignant mesothelioma (MM) is a rare but deadly malignancy with about 3,000 new cases being diagnosed each year in the US. Very...
Wed Nov 20, 2019 13:07
Related ArticlesLongitudinal Extensive Transverse Myelitis in an Immunocompetent Older Individual-A Rare Complication of Varicella-Zoster Virus Reactivation. Medicina (Kaunas). 2019 May 23;55(5): Authors: Abbas SA, El Helou J, Chalah MA, Hilal H, Saliba G, Abboud H, Ayache SS Abstract Varicella-zoster virus (VZV) is a human neurotropic herpes virus that causes chickenpox in children. After becoming latent in dorsal root ganglia, it can reactivate to...
Wed Nov 20, 2019 13:07
Related ArticlesAcute Tubulointerstitial Nephritis: A Case Report on Rare Adverse Effect of Pembrolizumab. Medicina (Kaunas). 2019 May 21;55(5): Authors: Basnet S, Dhital R, Tharu B Abstract Pembrolizumab is a novel immune checkpoint inhibitor approved for use in non-small cell lung carcinoma. There have been a few cases that have associated adverse renal outcomes with pembrolizumab. We present a case of acute kidney injury in a patient on pembrolizumab...
Wed Nov 20, 2019 13:07
Related ArticlesPeripheral adenomatoid odontogenic tumor in a cloak of an epulis: report of a rare case. BMC Oral Health. 2019 05 10;19(1):81 Authors: Dwivedi D, Prabhakar N, Kasetty S, Ahuja R Abstract BACKGROUND: Adenomatoid odontogenic tumor constitutes an uncommon benign odontogenic tumor which is well-known as "two-thirds tumor" (two-thirds of adenomatoid tumors occur in the maxilla, two-thirds occur in young females, two-thirds of the cases are...
Wed Nov 20, 2019 13:07
Related ArticlesNasal Chondrosarcoma of the Lower Lateral Cartilage. Medicina (Kaunas). 2019 May 09;55(5): Authors: Tan HB, Rimmer J Abstract Head and neck chondrosarcomas are incredibly rare with documented cases arising from skull base, maxilla, larynx, and nasal septum. We present the first reported case of chondrosarcoma arising from the lower lateral cartilage of the nose treated with surgical resection and primary reconstruction.PMID: 31075970...
Wed Nov 20, 2019 13:07
Related ArticlesHodgkin lymphoma transformation of chronic lymphocytic leukemia-A real life data from the Polish Lymphoma Research Group. Hematol Oncol. 2019 Oct;37(4):383-391 Authors: Drozd-Sokołowska J, Zaucha JM, Żółtak T, Jamroziak K, Grzybowska-Izydorczyk O, Witkowska M, Waszczuk-Gajda A, Kaźmierczak M, Szczepaniak A, Subocz E, Knopińska-Posłuszny W, Hołojda J, Kopińska A, Hus I, Rybka J, Wołowiec D, Kwiatkowski J, Hałaburda K, Smolewski P, Giebel S, Wiktor-Jędrzejczak...
Wed Nov 20, 2019 13:07
Related ArticlesMoxetumomab pasudotox: A first-in-class treatment for hairy cell leukemia. J Oncol Pharm Pract. 2019 Sep;25(6):1467-1472 Authors: Fancher KM, Lally-Montgomery ZC Abstract Hairy cell leukemia is a rare indolent B-cell lymphoid malignancy. Durable remission can be obtained with purine analogues, but relapse is inevitable, and effective treatment options may be limited. Moxetumomab pasudotox is a recombinant CD22-targeting immunotoxin that...
Wed Nov 20, 2019 13:07
Related ArticlesCase series of dabrafenib-trametinib-induced pyrexia successfully treated with colchicine. Support Care Cancer. 2019 Oct;27(10):3869-3875 Authors: Vera J, Paludo J, Kottschade L, Brandt J, Yan Y, Block M, McWilliams R, Dronca R, Loprinzi C, Grothey A, Markovic SN Abstract The most common adverse event (AE) of dabrafenib and trametinib (DT) is pyrexia, which has been reported to occur in up to 71% of patients. Pyrexia resulted in therapy...
Wed Nov 20, 2019 13:07
Related ArticlesIbrutinib for the treatment of Bing-Neel syndrome, a complication of Waldenström macroglobulinemia: Patient case report. J Oncol Pharm Pract. 2019 Sep;25(6):1534-1539 Authors: Hartsell L, Janes A, Larck C, Park S, Arnall JR Abstract Bing-Neel syndrome is a rare complication of Waldenström macroglobulinemia, characterized by infiltration of lymphoplasmacytic cells to the central nervous system. Multiple treatment modalities exist including...
Wed Nov 20, 2019 13:07
Related ArticlesAssessing the Pathogenicity, Penetrance, and Expressivity of Putative Disease-Causing Variants in a Population Setting. Am J Hum Genet. 2019 02 07;104(2):275-286 Authors: Wright CF, West B, Tuke M, Jones SE, Patel K, Laver TW, Beaumont RN, Tyrrell J, Wood AR, Frayling TM, Hattersley AT, Weedon MN Abstract More than 100,000 genetic variants are classified as disease causing in public databases. However, the true penetrance of many of...
Wed Nov 20, 2019 13:07
Related ArticlesOlder Age and Disease Duration Are Highly Associated with Hepatocellular Carcinoma in Patients with Autoimmune Hepatitis. Dig Dis Sci. 2019 06;64(6):1705-1710 Authors: Dakhoul L, Jones KR, Gawrieh S, Ghabril M, McShane C, Vuppalanchi R, Vilar-Gomez E, Nephew L, Chalasani N, Lammert C Abstract BACKGROUND: Hepatocellular carcinoma (HCC) is rare in patients with autoimmune hepatitis (AIH). However, the overall burden of AIH cirrhosis in...
Wed Nov 20, 2019 13:07
Related ArticlesClinicopathological and molecular analysis of multinodular and vacuolating neuronal tumors of the cerebrum. Hum Pathol. 2019 04;86:203-212 Authors: Choi E, Kim SI, Won JK, Chung CK, Kim SK, Choi SH, Choi S, Han B, Ahn B, Im SW, Park SH Abstract Multinodular and vacuolating neuronal tumor (MVNT) of the cerebrum is a recently recognized rare neuronal tumor, and its pathogenesis is unclear. We analyzed 7 cases of histologically typical...
Wed Nov 20, 2019 13:07
Related ArticlesMolecular characterization of metaplastic breast carcinoma via next-generation sequencing. Hum Pathol. 2019 04;86:85-92 Authors: Zhai J, Giannini G, Ewalt MD, Zhang EY, Invernizzi M, Niland J, Lai LL Abstract Metaplastic breast carcinoma (MBC) is a rare subtype of breast cancer with variable morphology. MBC is more often triple negative (ER-, PR-, HER2-) and is associated with poorer clinical outcome when compared with infiltrating ductal...
Wed Nov 20, 2019 13:07
Related ArticlesMolecular features of pleomorphic xanthoastrocytoma. Hum Pathol. 2019 04;86:38-48 Authors: Zou H, Duan Y, Wei D, Zhang Y, Dai J, Li J, Li X, Zhou J, Liu Z, Jin Z, Zhang Z, Yu Y, Hu Z Abstract Pleomorphic xanthoastrocytoma (PXA) is a rare central nervous system tumor occurring mostly in children and young adults. Next-generation sequencing of 295 cancer-related genes was used to investigate the molecular profiles of 13 cases of PXA. We...
Wed Nov 20, 2019 13:07
Related ArticlesRare but Recurrent ROS1 Fusions Resulting From Chromosome 6q22 Microdeletions are Targetable Oncogenes in Glioma. Clin Cancer Res. 2018 12 15;24(24):6471-6482 Authors: Davare MA, Henderson JJ, Agarwal A, Wagner JP, Iyer SR, Shah N, Woltjer R, Somwar R, Gilheeney SW, DeCarvalo A, Mikkelson T, Van Meir EG, Ladanyi M, Druker BJ Abstract PURPOSE: Gliomas, a genetically heterogeneous group of primary central nervous system tumors, continue...
Wed Nov 20, 2019 13:07
KMT2C Mutations in Diffuse-Type Gastric Adenocarcinoma Promote Epithelial-to-Mesenchymal Transition.
Related ArticlesKMT2C Mutations in Diffuse-Type Gastric Adenocarcinoma Promote Epithelial-to-Mesenchymal Transition. Clin Cancer Res. 2018 12 15;24(24):6556-6569 Authors: Cho SJ, Yoon C, Lee JH, Chang KK, Lin JX, Kim YH, Kook MC, Aksoy BA, Park DJ, Ashktorab H, Smoot DT, Schultz N, Yoon SS Abstract PURPOSE: Lauren diffuse-type gastric adenocarcinomas (DGAs) are generally genomically stable. We identified lysine (K)-specific methyltransferase 2C (KMT2C)...
Wed Nov 20, 2019 13:07
Related ArticlesLong-lasting response with polycythemia to third-line axitinib treatment in metastatic renal cell carcinoma: Very rare case presentation. J Oncol Pharm Pract. 2019 Sep;25(6):1512-1515 Authors: Dulgar O, Cil I, Zirtiloglu A, Tural D Abstract INTRODUCTION: Clear cell renal cell carcinoma is characterized by mutation or inactivation of Von Hippel-Lindau suppressor gene. The mutation of Von Hippel-Lindau mechanism is associated with the...
Wed Nov 20, 2019 13:07
Related ArticlesCerebral aspergillosis in a patient on ibrutinib therapy-A predisposition not to overlook. J Oncol Pharm Pract. 2019 Sep;25(6):1486-1490 Authors: Faisal MS, Shaikh H, Khattab A, Albrethsen M, Fazal S Abstract Ibrutinib has revolutionized the treatment of B-cell malignancies since its approval for chronic lymphocytic leukemia. It is also used in mantle cell lymphoma, diffuse large B-cell lymphoma, Waldenstrom's macroglobulinemia, among...
Wed Nov 20, 2019 13:07
Related ArticlesContained right atrial rupture: an unusual presentation of a rare primary cardiac tumour. Eur Heart J. 2018 05 01;39(17):1574-1575 Authors: Lane CE, Diaz Soto JC, Padang R, Luis SA PMID: 29529184 [PubMed - indexed for MEDLINE]
Wed Nov 20, 2019 13:07
Related Articles[Mixed epithelial and stromal tumour of the kidney: a case report]. Aktuelle Urol. 2018 Sep;49(5):429-432 Authors: Brüwer G, Naumann CM, V Petersdorff M, Jünemann K, Osmonov D Abstract Mixed epithelial and stromal tumours of the kidney are rare. Histologically, they are characterised by a complex of epithelium and stroma with cystic and solid areas. They usually occur in perimenopausal women receiving hormone replacement with oestrogen....
Wed Nov 20, 2019 13:07
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