Related ArticlesA rare case of Japanese encephalitis-induced anti-N-methyl-d-aspartate receptor encephalitis. Neurol India. 2018 Sep-Oct;66(5):1495-1496 Authors: Shaik RS, Netravathi M, Nitish LK, Mani RS, Shah P, Damodar T, Anita M, Pal PK PMID: 30233032 [PubMed - indexed for MEDLINE]
Thu Sep 19, 2019 13:24
Related ArticlesMedulloblastoma with extensive nodularity: A rare variant with a favorable outcome. Neurol India. 2018 Sep-Oct;66(5):1517-1518 Authors: Jakati S, Jyotsna RY, Purohit AK, Sundaram C PMID: 30233042 [PubMed - indexed for MEDLINE]
Thu Sep 19, 2019 13:24
Related ArticlesIdentification of therapeutic targets in chordoma through comprehensive genomic and transcriptomic analyses. Cold Spring Harb Mol Case Stud. 2018 12;4(6): Authors: Liang WS, Dardis C, Helland A, Sekar S, Adkins J, Cuyugan L, Enriquez D, Byron S, Little AS Abstract Chordoma is a rare, orphan cancer arising from embryonal precursors of bone. Surgery and radiotherapy (RT) provide excellent local control, often at the price of significant...
Thu Sep 19, 2019 13:24
Related ArticlesPrimary solitary extramedullary plasmacytoma progressing to multiple bone plasmacytomas: a rare condition with therapeutic dilemmas. Pol Arch Intern Med. 2018 11 30;128(11):706-708 Authors: Suska A, Chmura Ł, Dyduch G, Małkowski B, Jurczyszyn A AbstractPMID: 30335051 [PubMed - indexed for MEDLINE]
Thu Sep 19, 2019 13:24
Related ArticlesMismatch repair deficiency is a rare but putative therapeutically relevant finding in non-liver fluke associated cholangiocarcinoma. Br J Cancer. 2019 01;120(1):109-114 Authors: Goeppert B, Roessler S, Renner M, Singer S, Mehrabi A, Vogel MN, Pathil A, Czink E, Köhler B, Springfeld C, Pfeiffenberger J, Rupp C, Weiss KH, Schirmacher P, von Knebel Doeberitz M, Kloor M Abstract BACKGROUND: A major molecular pathway of genetic instability...
Thu Sep 19, 2019 13:24
Related ArticlesA rare complication of bone marrow aspiration and trephine biopsy: Staphylococcus aureus osteomyelitis and septicaemia. Br J Haematol. 2019 01;184(1):7 Authors: Khakwani M, Srinath S, Pratt G, Moss P PMID: 30408144 [PubMed - indexed for MEDLINE]
Thu Sep 19, 2019 13:24
Related ArticlesThe translational science of hodgkin lymphoma. Br J Haematol. 2019 01;184(1):30-44 Authors: Cirillo M, Reinke S, Klapper W, Borchmann S Abstract Hodgkin Lymphoma (HL) is an unusual B-cell lymphoma because the malignant cells exist as a minority population in a densely cellular microenvironment. The microenvironment is comprised predominately of inflammatory and immune cells with fibrosis in some cases. There are multiple dysregulated...
Thu Sep 19, 2019 13:24
Related ArticlesMesothelial cyst of the round ligament. G Chir. 2018 Sep-Oct;34(5):323-325 Authors: Apostolakis S, Ioannidis A, Koutserimpas C, Patrikakos P, Perrakis A, Velimezis G Abstract Mesothelial cyst of the round ligament is a rare finding in females, with only a few cases reported so far. A case of a 25 year old female patient presenting with a palpable mass in her right inguinal region is presented. The preoperative investigation through ultrasound...
Thu Sep 19, 2019 13:24
Related ArticlesWhole-genome and transcriptome profiling of a metastatic thyroid-like follicular renal cell carcinoma. Cold Spring Harb Mol Case Stud. 2018 12;4(6): Authors: Ko JJ, Grewal JK, Ng T, Lavoie JM, Thibodeau ML, Shen Y, Mungall AJ, Taylor G, Schrader KA, Jones SJM, Kollmannsberger C, Laskin J, Marra MA Abstract Thyroid-like follicular renal cell carcinoma (TLFRCC) is a rare cancer with few reports of metastatic disease. Little is known regarding...
Thu Sep 19, 2019 13:24
Related ArticlesModern principles in the management of nodular lymphocyte-predominant Hodgkin lymphoma. Br J Haematol. 2019 01;184(1):17-29 Authors: Spinner MA, Varma G, Advani RH Abstract Nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) is a unique rare subtype of Hodgkin lymphoma (HL) which differs clinically, pathologically and biologically from classic HL, warranting a nuanced approach to treatment. CD20 expression by malignant lymphocyte-predominant...
Thu Sep 19, 2019 13:24
Related ArticlesEncephalitis with anti-NMDA receptor antibodies: paraneoplastic or non-paraneoplastic? Neuro Endocrinol Lett. 2018 Dec;39(5):351-354 Authors: Masopust J, Tvaroh A, Pavelek Z, Valis M Abstract We report the case of an encephalitis patient with anti-N-methyl-D-aspartate receptor (NMDAR) antibody positivity. Anti-NMDAR encephalitis is a relatively rare autoimmune disease. In our patient, the diagnosis of anti-NMDAR encephalitis was established...
Thu Sep 19, 2019 13:24
Related ArticlesO6-methylguanine-DNA methyltransferase (MGMT) status in neuroendocrine tumors: a randomized phase II study (MGMT-NET). Dig Liver Dis. 2019 04;51(4):595-599 Authors: Lemelin A, Barritault M, Hervieu V, Payen L, Péron J, Couvelard A, Cros J, Scoazec JY, Bin S, Villeneuve L, Lombard-Bohas C, Walter T, MGMT-NET investigators Abstract INTRODUCTION: Neuroendocrine tumors (NETs) are rare, but their incidence is rising. Alkylating agents (ALKY),...
Thu Sep 19, 2019 13:24
Related ArticlesMANAGEMENT OF ENDOCRINE DISEASE: Unmet therapeutic, educational and scientific needs in parathyroid disorders. Eur J Endocrinol. 2019 09 01;181(3):P1-P19 Authors: Bollerslev J, Schalin-Jantti C, Rejnmark L, Siggelkow H, Morreau H, Thakker RV, Sitges-Serra A, Cetani F, Marcocci C, PARAT Workshop Group Abstract PARAT, a new European Society of Endocrinology program, aims to identify unmet scientific and educational needs of parathyroid...
Thu Sep 19, 2019 13:24
Related Articles[EXIT: Experiences from Karolinska University Hopsital]. Lakartidningen. 2019 May 15;116: Authors: Mesas Burgos C, Tiblad E, Papatziamos G, Jörnvall H, Conner P Abstract The main, but not sole, indication for an Ex-utero Intrapartum Treatment (EXIT) delivery is an airway obstruction due to either laryngeal atresia or tumors in the head and neck region. Here we present our Institution's experience with eleven cases: three teratomas, four...
Thu Sep 19, 2019 13:24
Related ArticlesNovel technique using tensor fascia lata graft to reconstruct a floor of mouth postablative defect from invasive ectopic papillary carcinoma of the thyroglossal duct tract. Ann R Coll Surg Engl. 2019 Sep;101(7):e160-e163 Authors: Izadi D, Al-Zahid S, Smith J, Wallace CG Abstract We describe a rare case of ectopic papillary thyroid cancer in the thyroglossal duct tract invading the floor-of-mouth musculature. The postablative defect was...
Thu Sep 19, 2019 13:24
Related Articles[Upper urinary tract tumor and hydronephrosis to pelviureteric junction obstruction: a rare association]. Pan Afr Med J. 2018;31:201 Authors: Ennaciri S, Omana JP Abstract The association between tumor of the urinary tract and hydronephrosis caused by a syndrome of the pyelo-ureteral junction is rare. Indeed, tumors of the upper urinary tract and hydronephrosis have generally a cause-effect relationship. This last is due, more often,...
Thu Sep 19, 2019 13:24
Related Articles[Solid pseudo-papillary tumor of the pancreas]. Pan Afr Med J. 2018;31:212 Authors: Maghrebi H, Makni A, Rehaim R, Haddad A, Rebai W, Ayadi M, Daghfous A, Fteriche F, Chebbi F, Ksantini R, Jouini M, Kacem M, Safta ZB Abstract Solid pseudo-papillary tumors of the pancreas (SPTP) are rare epithelial tumors. In most cases, they occur in young woman in the second or the third decades of life. Survival after primary resection is approximatively...
Thu Sep 19, 2019 13:24
Related ArticlesFertility sparing surgery for ovarian sex cord stromal tumors: a nine case series. Pan Afr Med J. 2018;31:221 Authors: Ghalleb M, Bouzaiene H, Sghaier S, Bouaziz H, Hechiche M, Hassouna JB, Rahal K Abstract Ovarian Sex Cord Stromal Tumors (SCST) are a rare disease carrying a good prognosis. They generally affect young women; therefore fertility preservation is a critical issue. Fertility Sparing Surgery (FSS) showed promising results...
Thu Sep 19, 2019 13:24
Related ArticlesLeiomyosarcoma of scrotum: case report. Pan Afr Med J. 2018;31:238 Authors: Bouhout T, Serji B, Egyir EU, Amri BE, Bouhout I, Soufi M, Bouziane M, Harroudi TE Abstract Scrotal leiomyosarcoma is rare tumor. It presents as a painless, slow-growing cutaneous lesion. It's often mistaken for a benign condition. It is best treated by wide local excision. A case of scrotum leiomyosarcoma is presented in a 63 year old patient who was treated...
Thu Sep 19, 2019 13:24
Related Articles[Giant subcutaneous metastasis originating from vesicular thyroid carcinoma: about a case]. Pan Afr Med J. 2018;31:245 Authors: Andrianandrasana NOT, Razakanaivo M, Rahantamalala MI, Rafaramino FJ Abstract Secondary subcutaneous metastasis originating from vesicular thyroid carcinoma is unusual. It accounts for more than 5.8% of most common sites of metastasis for thyroid carcinoma. We here report the case of a 60-year old woman presenting...
Thu Sep 19, 2019 13:24
Related Articles[Squamous cells carcinoma of the renal pelvis discovered due to parietal and skin invasion: an uncommon manifestation]. Pan Afr Med J. 2018;31:246 Authors: Slimane M, Hadidane M, Bouzaiene H, Driss M, Jaidane O, Henchiri H, Hechiche M, Rahal K Abstract We here report a rare case of squamous cells carcinoma of the renal pelvis with abdominal wall skin invasion in a patient with a history of recurrent upper urinary tract infections due...
Thu Sep 19, 2019 13:24
Related ArticlesAmeloblastic carcinoma: a clinicopathologic analysis of cases seen in a Nigerian Teaching Hospital and review of literature. Pan Afr Med J. 2018;31:208 Authors: Soyele OO, Adebiyi KE, Adesina OM, Ladeji AM, Aborisade A, Olatunji A, Adeola HA Abstract Introduction: Ameloblastic carcinoma is a rare malignant odontogenic neoplasm that exhibits histological features of ameloblastoma in combination with cytological atypia. It may arise de...
Thu Sep 19, 2019 13:24
Related Articles[Clinical characteristics of lung NK/T cell lymphoma misdiagnosed as pneumonia]. Zhonghua Yi Xue Za Zhi. 2019 Sep 10;99(34):2696-2700 Authors: Wu J, Qiu YJ, Xu AG, Xing LH, Zhang QX Abstract Objective: To investigate the clinical features of lung natural killer (NK)/T cell lymphoma. Methods: The clinical data of patients with lung NK/T-cell lymphoma confirmed by pathology who were hospitalized due to lung shadow and initially treated...
Thu Sep 19, 2019 13:24
Related Articles[Ectopic Hilar Thymoma Associated with Morvan Syndrome after Extended Thymectomy for Myasthenia Gravis]. Kyobu Geka. 2019 Sep;72(9):660-663 Authors: Shimazu Y, Tanaka H, Watanabe H, Yamazaki N, Nakade M Abstract Morvan syndrome is a rare autoimmune neurological disease characterized by peripheral nerve hyperexcitability, autonomic dysfunction and encephalopathy. Morvan syndrome is often associated with thymoma as a paraneoplastic condition....
Thu Sep 19, 2019 13:24
Related Articles[Multiple Primary Pulmonary Meningiomas]. Kyobu Geka. 2019 Sep;72(9):677-680 Authors: Sakai K, Someya T, Kasahara I, Itou E, Shirai T Abstract We report a rare case of multiple primary pulmonary meningiomas in a 52-year-old woman who presented with lung nodules identified on abdominal computed tomography(CT). She had a history of surgery and chemotherapy for an immature ovarian teratoma 33 years prior to presentation. She underwent resection...
Thu Sep 19, 2019 13:24
Related ArticlesAAGAB Mutations in 18 Canadian Families With Punctate Palmoplantar Keratoderma and a Possible Link to Cancer. J Cutan Med Surg. 2019 Sep 16;:1203475419878161 Authors: Elhaji Y, Hedlin C, Nath A, Price EL, Gallant C, Northgrave S, Hull PR Abstract BACKGROUND: Punctate palmoplantar keratoderma type 1 (PPPK1) presents in late childhood to adulthood with multiple small discrete hyperkeratotic papules on palms and soles. PPPK1 is an autosomal...
Thu Sep 19, 2019 13:24
Related Articles[Comparison of Effectiveness of Gefitinib, Erlotinib, and Afatinib in Advanced Non-small Cell Lung Cancer Patients with EGFR Mutation Positive in Indonesian Population]. Zhongguo Fei Ai Za Zhi. 2019 Sep 20;22(9):562-567 Authors: Sutandyo N, Hanafi A, Jayusman M Abstract BACKGROUND: EGFR-tyrosine kinase inhibitors (EGFR-TKIs) were used to treat non-small cell lung cancer (NSCLC) patients with EGFR mutation positive. This study aims to...
Thu Sep 19, 2019 13:24
Related Articles[A Review of EGFR-TKIs Therapy of Non-small Cell Lung Cancer
with Uncommon EGFR Mutations]. Zhongguo Fei Ai Za Zhi. 2019 Sep 20;22(9):590-599 Authors: Du W, Wo Y, Lu T, Wang Y, Jiao W Abstract Lung cancer is the most common cancer and the leading cause of cancer death. Non-small cell lung cancer (NSCLC) represents over 85% of all lung cancers, and up to 50% of Asian NSCLC patients harboring epidermal growth factor receptor (EGFR) gene...
Thu Sep 19, 2019 13:24
Related ArticlesIncidental endobronchial hamartoma in a patient with enchondroma. BMJ Case Rep. 2019 Sep 16;12(9): Authors: Kadamkulam Syriac A, Bhaskarla AV, Elrifai M, Alraiyes AH Abstract Hamartomas are the most common type of benign tumours of the lung, constituting a small portion of all lung neoplasms. Hamartomas are rare benign tumours composed of multiple mesenchymal cell lines. Two clinical types have been defined according to the location:...
Thu Sep 19, 2019 13:24
Related ArticlesImpact of Surgery on Long-Term Results of Hearing in Neurofibromatosis Type-2 Associated Vestibular Schwannomas. Cancers (Basel). 2019 Sep 16;11(9): Authors: Gugel I, Grimm F, Liebsch M, Zipfel J, Teuber C, Kluwe L, Mautner VF, Tatagiba M, Schuhmann MU Abstract Hearing preservation is a major goal in the treatment of neurofibromatosis type 2 (NF2) associated vestibular schwannoma (VS), particularly in children and adolescents. In this...
Thu Sep 19, 2019 13:24
Related ArticlesEstimating cumulative point prevalence of rare diseases: analysis of the Orphanet database. Eur J Hum Genet. 2019 Sep 16;: Authors: Nguengang Wakap S, Lambert DM, Olry A, Rodwell C, Gueydan C, Lanneau V, Murphy D, Le Cam Y, Rath A Abstract Rare diseases, an emerging global public health priority, require an evidence-based estimate of the global point prevalence to inform public policy. We used the publicly available epidemiological data...
Thu Sep 19, 2019 13:24
Related ArticlesDiagnosis and management of pancreatic cystic neoplasms: current evidence and guidelines. Nat Rev Gastroenterol Hepatol. 2019 Sep 16;: Authors: van Huijgevoort NCM, Del Chiaro M, Wolfgang CL, van Hooft JE, Besselink MG Abstract Pancreatic cystic neoplasms (PCN) are a heterogeneous group of pancreatic cysts that include intraductal papillary mucinous neoplasms, mucinous cystic neoplasms, serous cystic neoplasms and other rare cystic lesions,...
Thu Sep 19, 2019 13:24
Related ArticlesPrimary Squamous Cell Carcinoma of the Thyroid. Ochsner J. 2019;19(3):290-292 Authors: Raggio B, Barr J, Ghandour Z, Friedlander P Abstract Background: Primary squamous cell carcinoma of the thyroid (PSCCT) is a rare malignancy of the head and neck, with fewer than 60 cases reported in the literature. We report a case of PSCCT and provide a brief review of the literature. Case Report: A 66-year-old female with a history of a hemithyroidectomy...
Thu Sep 19, 2019 13:24
Related ArticlesAn unusual site of metastasis from carcinoma of tongue - metastasis to lumbar vertebrae: A case report and review of literature. Surg Neurol Int. 2019;10:33 Authors: Beniwal M, Vikas V, Rao KVLN, Srinivas D, Sampath S Abstract Background: Carcinoma of tongue is a common site of oral cancer. It usually occurs at mean age of 61.1 years and is more common in males when compared with females. It commonly spreads directly and through lymphatics...
Thu Sep 19, 2019 13:24
Related ArticlesSuprasellar pleomorphic xanthoastrocytoma: A case report. Surg Neurol Int. 2019;10:72 Authors: Telemi E, Martirosyan NL, J Avila M, Lukefahr AL, Le C, Lemole GM Abstract Background: Pleomorphic xanthoastrocytoma (PXA) is a rare form of astrocytic neoplasm most commonly found in children and young adults. This neoplasm, which is classified as a Grade II tumor by the World Health Organization classification of tumors of the central nervous...
Thu Sep 19, 2019 13:24
Related ArticlesWhen Adenocarcinoma Went Hand in Hand with Neuroendocrine Tumor: A Rare Case of Adenocarcinoma Synchronous with Neuroendocrine Tumor in Ampulla of Vater. Cureus. 2019 Jul 18;11(7):e5168 Authors: Kochar T, Dhingra P, Shah H Abstract Neuroendocrine tumors (NETs) of gastrointestinal tract are rare entities. Their presence as synchronous lesions with adenocarcinoma has rarely been described in the literature. Cases of synchronous lesions...
Thu Sep 19, 2019 13:24
Related ArticlesPrimary pulmonary undifferentiated pleomorphic sarcoma (PPUPS). Autops Case Rep. 2019 Jul-Sep;9(3):e2019110 Authors: Qorbani A, Nelson SD Abstract Undifferentiated pleomorphic sarcoma (UPS) is a high-grade pleomorphic neoplasm with no identifiable line(s) of differentiation using currently available diagnostic techniques. Therefore, it is essentially a diagnosis of exclusion, which requires generous tissue sampling, adequate contextually...
Thu Sep 19, 2019 13:24
Related Articles[Hepatic epithelioid angiomyolipoma/PEComa and focal nodular hyperplasia in a patient with a previous history of cutaneous melanoma]. Rev Esp Patol. 2019 Oct - Dec;52(4):250-255 Authors: Machado I, Marhuenda A, Trallero M, Caballero M, Santos J, Cruz J, Estevan R Abstract Hepatic perivascular epithelioid cell tumors (PEComas) are uncommon mesenchymal neoplasms. PEComas concurrent with other hepatic lesions is a very rare occurrence, with...
Thu Sep 19, 2019 14:23
Related Articles[A rare pathology of the petrous part of the temporal bone: adenoma of the middle ear]. HNO. 2019 Sep 17;: Authors: Sudhoff H, Gehl HB, Brasch F, Riemann R, Todt I Abstract Adenomas are very rare tumors of the middle ear. They are benign neoplasms originating from the glandular components of the mucous membrane of the middle ear. The middle ear adenoma was first described by Hyams and Michaels in 1976, which was named an adenomatous tumor....
Thu Sep 19, 2019 14:23
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