Salivary gland hyalinizing clear cell carcinoma with cutaneous metastasis: a rare and deceptive tumor. J Cutan Pathol. 2020 Jul 08;: Authors: Abou Shaar R, Zia S, Alhamar M, Romano T, Shaw B, Keller C, Friedman BJ Abstract Clear cell carcinoma (CCC) is an uncommon malignant tumor of minor salivary glands. It characteristically has a low-grade morphology and a favorable outcome by most reports. An EWSR1-ATF1 fusion can be detected in the majority...
Thu Jul 09, 2020 13:40
Single-cell genomics reveals the genetic and molecular bases for escape from mutational epistasis in myeloid neoplasms. Blood. 2020 Jul 08;: Authors: Taylor J, Mi X, North KD, Binder M, Penson A, Lasho TL, Knorr K, Haddadin M, Liu B, Pangallo J, Benbarche S, Wiseman DH, Tefferi A, Halene S, Liang Y, Patnaik MM, Bradley RK, Abdel-Wahab O Abstract Large-scale sequencing studies of hematologic malignancies have revealed notable epistasis among...
Thu Jul 09, 2020 13:40
Telemedicine During the COVID-19 Pandemic: Impact on Care for Rare Cancers. JCO Glob Oncol. 2020 Jul;6:1046-1051 Authors: Smrke A, Younger E, Wilson R, Husson O, Farag S, Merry E, Macklin-Doherty A, Cojocaru E, Arthur A, Benson C, Miah AB, Zaidi S, Gennatas S, Jones RL Abstract PURPOSE: Many patients with cancer, often those with rare cancers such as sarcomas, travel long distances to access expert care. The COVID-19 pandemic necessitated widespread...
Thu Jul 09, 2020 13:40
Gene Fusion Characterization of Rare Aggressive Prostate Cancer Variants - Adenosquamous Carcinoma, Pleomorphic Giant Cell Carcinoma, and Sarcomatoid Carcinoma: An Analysis of 19 Cases. Histopathology. 2020 Jul 08;: Authors: Alhamar M, Vladislav T, Smith SC, Gao Y, Cheng L, Favazza LA, Alani AM, Ittmann MM, Riddle ND, Whiteley LJ, Gupta NS, Carskadon S, Gomez-Gelvez JC, Chitale DA, Palanisamy N, Hes O, Trpkov K, Williamson SR Abstract AIMS:...
Thu Jul 09, 2020 13:40
Carbonic Anhydrase IX (CA9) Expression in Multiple Renal Epithelial Tumor Subtypes. Histopathology. 2020 Jul 08;: Authors: Baniak N, Flood TA, Buchanan M, Dal Cin P, Hirsch MS Abstract AIMS: Renal epithelial neoplasms (RENs) can be difficult to subclassify due to overlapping morphologic features. Carbonic anhydrase 9 (CA9) is a common biomarker for clear cell renal cell carcinoma (CCRCC); however, sensitivity and specificity across REN subtypes...
Thu Jul 09, 2020 13:40
Related Articles Breast Cancer With a HER2 IHC2+ and FISH HER2/CEP17 Ratio ≥2.0 and an Average HER2 Gene Copy Number <4.0 per Tumor Cell: HER2 mRNA Overexpression Is a Rare Event. Front Oncol. 2020;10:985 Authors: Liu Y, Wu S, Shi X, Mao F, Zeng X Abstract Purpose: For breast cancer, accurately illustrating HER2 characteristics is a critical precondition for evaluating the prognosis and predicting the efficacy of anti-HER2 therapy. Our purpose...
Thu Jul 09, 2020 13:40
Related Articles Genomics of Peripheral T-Cell Lymphoma and Its Implications for Personalized Medicine. Front Oncol. 2020;10:898 Authors: Zhang Y, Lee D, Brimer T, Hussaini M, Sokol L Abstract Peripheral T-cell lymphoma (PTCL) is a rare, heterogenous group of mature T-cell neoplasms that comprise 10-15% of non-Hodgkin lymphoma cases in the United States. All subtypes of PTCL, except for ALK+ anaplastic T-cell lymphoma, are associated with poor...
Thu Jul 09, 2020 13:40
Related Articles Polycythemia Vera Presenting With Normal Hemoglobin and Hematocrit: A Rare Variant. Cureus. 2020 Jun 02;12(6):e8404 Authors: Erdinc B, Ramachandran P, Boris A Abstract Polycythemia vera (PV) is a myeloproliferative neoplasm, and its diagnosis requires elevated hemoglobin level (>16.5 mg/dL in men and >16 mg/dL in women), bone marrow characteristics of PV (hypercellularity for age with trilineage growth), and presence of...
Thu Jul 09, 2020 13:40
Related Articles Prefibrotic Myelofibrosis Presenting with Multiple Cerebral Embolic Infarcts and the Rare MPL W515S Mutation. Case Rep Hematol. 2020;2020:8375986 Authors: Langabeer SE, Lee Tokar L, Kearney L, O'Brien C, Thavarajah K, Barrett A, McManus J, O'Leary H Abstract Acquired, activating mutations of MPL W515 are recognised driver mutations of the myeloproliferative neoplasms (MPN), namely, essential thrombocythemia and primary myelofibrosis....
Thu Jul 09, 2020 13:40
Related Articles Adenoid Cystic Carcinoma of Salivary Gland: A Ten-Year Single Institute Experience. Curr Health Sci J. 2020 Jan-Mar;46(1):56-65 Authors: Belulescu IC, Margaritescu C, Dumitrescu CI, DĂguci L, Munteanu C, Margaritescu OC Abstract Adenoid cystic carcinoma is a rare tumor, accounting for about 7.5% of all salivary gland neoplasms. More frequent developing in minor salivary gland, this is a slow-growing tumor with a long-lasting...
Thu Jul 09, 2020 13:40
Related Articles Pathophysiology of paraneoplastic and autoimmune encephalitis: genes, infections, and checkpoint inhibitors. Ther Adv Neurol Disord. 2020;13:1756286420932797 Authors: Vogrig A, Muñiz-Castrillo S, Desestret V, Joubert B, Honnorat J Abstract Paraneoplastic neurological syndromes (PNSs) are rare complications of systemic cancers that can affect all parts of the central and/or peripheral nervous system. A body of experimental and...
Thu Jul 09, 2020 13:40
Related Articles Germline Sequencing Identifies Rare Variants in Finnish Subjects with Familial Germ Cell Tumors. Appl Clin Genet. 2020;13:127-137 Authors: Crowgey EL, Soini T, Shah N, Pauniaho SL, Lahdenne P, Wilson DB, Heikinheimo M, Druley TE Abstract Purpose: Pediatric germ cell tumors are rare, representing about 3% of childhood malignancies in children less than 15 years of age, presenting in neonates or adolescents with a greater incidence...
Thu Jul 09, 2020 13:40
Related Articles Histopathologic features of breast cancer in Li-Fraumeni syndrome. Mod Pathol. 2020 Jul 07;: Authors: Kuba MG, Lester SC, Bowman T, Stokes SM, Taneja KL, Garber JE, Dillon DA Abstract Breast cancer is the most common malignancy in female patients with Li-Fraumeni syndrome (LFS), a rare autosomal dominant hereditary syndrome characterized by germline TP53 mutations. Recent studies have shown that the majority of these tumors...
Thu Jul 09, 2020 13:40
Related Articles Paraplegia Caused by Spontaneous Spinal Hemorrhage in a Patient Undergoing Rivaroxaban Therapy. Am J Case Rep. 2020 Jul 07;21:e923607 Authors: Feret WB, Kwiatkowska E, Domański L Abstract BACKGROUND Spinal hematomas can be post-traumatic, iatrogenic, or spontaneous. A spontaneous spinal hematoma is a rare finding, but one with very serious clinical implications. There are some risk factors linked to its occurrence, e.g. arteriovenous...
Thu Jul 09, 2020 13:40
Related Articles Gastric metastases from primary breast cancers: rare causes of common gastrointestinal disorders. BMJ Case Rep. 2020 Jul 06;13(7): Authors: Yuen T, Liu E, Kohansal A Abstract We report two cases of gastric metastases from primary breast cancers. In case 1, a 31-year-old woman with right-sided ductal breast carcinoma presented with nausea, vomiting and frank haematemesis, 8 months after mastectomy and adjuvant chemotherapy. An...
Thu Jul 09, 2020 13:40
Related Articles Extracerebral choroid plexus papilloma in the pharynx with airway obstruction in a newborn: a case report. BMC Pediatr. 2020 Jul 07;20(1):336 Authors: Lee N, Bae MH, Han YM, Park KH, Hwang JY, Hwang CS, Lee JC, Byun SY Abstract BACKGROUND: Choroid plexus papillomas (CPPs) are rare, usually benign, neoplasms originating in the central nervous system. In this study, we present the first case of a giant airway-obstructing CPP in...
Thu Jul 09, 2020 13:40
Related Articles HPV nonrelated endocervical adenocarcinoma in hereditary cancer syndromes. Tumori. 2020 Jul 08;:300891620936752 Authors: Carnevali I, Di Lauro E, Pensotti V, Sahnane N, Leoni E, Formenti G, Ghezzi F, Sessa F, Tibiletti MG Abstract INTRODUCTION: The relationship between endocervical cancer and cancer susceptibility syndromes is not yet fully understood. We present 2 cases of endocervical cancer: 1 arising in a patient carrier...
Thu Jul 09, 2020 13:40
Related Articles Rare exon 10 deletion in POLH gene in a family with xeroderma pigmentosum variant correlating with protein expression by immunohistochemistry. G Ital Dermatol Venereol. 2020 Jun;155(3):349-354 Authors: Borroni RG, Diegoli M, Grasso M, Concardi M, Agozzino M, Vignini M, Arbustini E Abstract Xeroderma pigmentosum (XP) is a rare autosomal recessive disease characterized by severe cutaneous and ocular sensitivity to sunlight, leading...
Thu Jul 09, 2020 13:40
Related Articles Characteristics and Outcome of Children with Renal Cell Carcinoma: A Narrative Review. Cancers (Basel). 2020 Jul 03;12(7): Authors: van der Beek JN, Geller JI, de Krijger RR, Graf N, Pritchard-Jones K, Drost J, Verschuur AC, Murphy D, Ray S, Spreafico F, Dzhuma K, Littooij AS, Selle B, Tytgat GAM, van den Heuvel-Eibrink MM Abstract Pediatric renal cell carcinoma (RCC) is a rare type of kidney cancer, most commonly occurring...
Thu Jul 09, 2020 13:40
Related Articles Merkel Cell Polyomavirus and Merkel Cell Carcinoma. Cancers (Basel). 2020 Jul 03;12(7): Authors: Pietropaolo V, Prezioso C, Moens U Abstract Viruses are the cause of approximately 15% of all human cancers. Both RNA and DNA human tumor viruses have been identified, with Merkel cell polyomavirus being the most recent one to be linked to cancer. This virus is associated with about 80% of Merkel cell carcinomas, a rare, but aggressive...
Thu Jul 09, 2020 13:40
Related Articles [Multifocal brain lesions]. Zh Nevrol Psikhiatr Im S S Korsakova. 2020;120(5):100-109 Authors: Abbasov FA, Bril EV, Zimnyakova OS, Marchenkova MS, Bashkov AN, Bogolepova EA, Davtyan AA, Lepsveridze LT, Semenov MS, Yusupova MM Abstract Despite the current laboratory and instrumental approaches to the diagnosis, a patient with multiple brain lesions remains a difficult one. The reason is that these lesions can be caused by a variety...
Thu Jul 09, 2020 13:40
Related Articles [Virus-induced opsoclonus-myoclonus syndrome during pregnancy]. Zh Nevrol Psikhiatr Im S S Korsakova. 2020;120(5):93-99 Authors: Alekseeva TM, Topuzova MP, Skripchenko NV, Simakov KV, Senkevich KA, Novozhilova MA, Agapova OY, Ternovykh IK, Chaykovskaya AD Abstract Opsoclonus-myoclonus syndrome (OMS) is a very rare condition with various etiologies (paraneoplastic, parainfectious, toxic, idiopathic, etc.) with an autoimmune pathogenetic...
Thu Jul 09, 2020 13:40
Related Articles A novel TJP1-ROS1 fusion in malignant peripheral nerve sheath tumor responding to crizotinib: A case report. Medicine (Baltimore). 2020 Jun 26;99(26):e20725 Authors: Li J, Liu L, Zhang Q, Huang Y, Zhang Y, Gan X, Liu S, Yue Z, Wei Y Abstract RATIONALE: Malignant peripheral nerve sheath tumor (MPNST) is a rare sarcoma. Owing to the lack of specific histological criteria, immunohistochemical, and molecular diagnostic markers,...
Thu Jul 09, 2020 13:40
Related Articles Tumour-to-tumour metastasis: breast carcinoma to an olfactory neuroblastoma. Ann R Coll Surg Engl. 2020 Jul;102(6):e118-e121 Authors: Bashyam A, Grammatopoulou V, Crook T, Di Palma S, Sunkaraneni VS Abstract Tumour-to-tumour metastasis is a rare phenomenon. It occurs when a primary tumour is a recipient of a separate tumour within the same individual. We present a case of a 66-year-old woman with known breast cancer who presented...
Thu Jul 09, 2020 13:40
Related Articles Campylobacter jejuni bacteremia in Italian pediatric patients with acute lymphoblastic leukemia: Report of two cases. New Microbiol. 2020 Apr;43(2):96-98 Authors: Martora F, Pagliuca C, Della Pepa ME, Della Rocca MT, Curto S, Iovene MR, Vitiello M Abstract Infections caused by Campylobacter jejuni are rarely associated with extraintestinal complications. C. jejuni bacteremia is difficult to detect in patients with hematological...
Thu Jul 09, 2020 13:40
Related Articles Bilateral giant parathyroid adenoma in the absence of multiple endocrine neoplasia type 1. Ann R Coll Surg Engl. 2020 Jul;102(6):e111-e114 Authors: Liu P, Vakharia N, Zacharia A, Rogers M, Tanweer F Abstract INTRODUCTION: Bilateral giant parathyroid adenoma in the absence of multiple endocrine neoplasia (MEN) type 1 is extremely rare and literature on this subject is limited. CASE HISTORY: A 79-year-old man presented...
Thu Jul 09, 2020 13:40
Related Articles A giant ganglioneuroma accompanied with scoliosis. Ann R Coll Surg Engl. 2020 Jul;102(6):e133-e135 Authors: Zhang Q, Li F, Liu D, Zhao S Abstract Ganglioneuroma is a rare benign neoplasm. Patients with ganglioneuroma show no symptoms. We describe a rare case of giant ganglioneuroma with scoliosis in a 35-year-old woman, who presented to our hospital for haemoptysis. We combined with neurosurgeons to remove the tumour successfully....
Thu Jul 09, 2020 13:40
Related Articles Cutaneous apocrine cystomatosis in three slaughter-aged pigs. J Vet Diagn Invest. 2020 Jan;32(1):159-161 Authors: López-Figueroa C, Domingo M, Martí B, Vidal E, Segalés J Abstract Apocrine cystomatosis is a rare condition characterized by clusters of cystically dilated sweat glands or other specialized apocrine glands. Cystic dilation of cutaneous sweat glands has been described in humans, dogs, and cats, but not in pigs, to...
Thu Jul 09, 2020 13:40
Related Articles Mediastinal Epithelioid Hemangioendothelioma Invading Superior Vena Cava: A Case Report and Review of Literature. Curr Med Imaging Rev. 2019;15(3):349-352 Authors: Kim SH, Kim YS, Jang MH, Kwon HJ Abstract INTRODUCTION: Epithelioid Hemangioendothelioma (EHE) is a rare vascular neoplasm. Common locations of EHE are the bone, soft tissue, liver, and lung, but the mediastinal location is extremely rare. Few cases of mediastinal...
Thu Jul 09, 2020 13:40
Related Articles State-of-the-art MR Imaging of Uncommon Hepatocellular Tumours: Fibrolamellar Hepatocellular Carcinoma and Combined Hepatocellularcholangiocarcinoma. Curr Med Imaging Rev. 2019;15(3):269-280 Authors: Anysz-Grodzicka A, Podgorska J, Cieszanowski A Abstract BACKGROUND: Fibrolamellar Carcinoma (FLC) and Combined Hepatocellular- Cholangiocarcinoma (CHC) are rare primary liver tumours, which are related to different clinical settings....
Thu Jul 09, 2020 13:40
Related Articles A Rare Instance of Primary Oncocytic Schneiderian Papilloma of Middle Ear and Eustachian Tube With a Combined Trans Oto and Nasal Approach Resection. J Craniofac Surg. 2020 Mar/Apr;31(2):504-506 Authors: Fu ZM, Zhao LP, Guo YY, Guan GF Abstract Oncocytic Schneiderian papillomas are rare tumours which usually arise in the sinonasal region. This paper presents, to the authors' knowledge, the first reported case of oncocytic Schneiderian...
Thu Jul 09, 2020 13:40
Related Articles Succinate dehydrogenase deficiency in a chromaffin cell model retains metabolic fitness through the maintenance of mitochondrial NADH oxidoreductase function. FASEB J. 2020 01;34(1):303-315 Authors: Kľučková K, Thakker A, Vettore L, Escribano-Gonzalez C, Hindshaw RL, Tearle JLE, Goncalves J, Kaul B, Lavery GG, Favier J, Tennant DA Abstract Mutations in succinate dehydrogenase (SDH) lead to the development of tumors in a restricted...
Thu Jul 09, 2020 13:40
Related Articles Adult stem cells and regenerative medicine-a symposium report. Ann N Y Acad Sci. 2020 02;1462(1):27-36 Authors: Cable J, Fuchs E, Weissman I, Jasper H, Glass D, Rando TA, Blau H, Debnath S, Oliva A, Park S, Passegué E, Kim C, Krasnow MA Abstract Adult stem cells are rare, undifferentiated cells found in all tissues of the body. Although normally kept in a quiescent, nondividing state, these cells can proliferate and differentiate...
Thu Jul 09, 2020 13:40
Related Articles Tumour response to TRK inhibition in a patient with pancreatic adenocarcinoma harbouring an NTRK gene fusion. Ann Oncol. 2019 11 01;30(Suppl_8):viii36-viii40 Authors: O'Reilly EM, Hechtman JF Abstract BACKGROUND: Although rare, NTRK gene fusions are known to be oncogenic drivers in pancreatic ductal adenocarcinoma (PDAC). We report the response of a metastatic CTRC-NTRK1 gene fusion-positive PDAC to targeted treatment with...
Thu Jul 09, 2020 13:40
Related Articles An unusual presentation of Sutton's phenomenon presenting as halo cherry angioma. J Eur Acad Dermatol Venereol. 2019 Dec;33(12):e464-e465 Authors: Amico S, Jacquemin C, Boniface K, Jullié ML, Taieb A, Seneschal J PMID: 31283033 [PubMed - indexed for MEDLINE]
Thu Jul 09, 2020 13:40
Related Articles Multiple endocrine neoplasia type 1 in Poland: a two-centre experience. Endokrynol Pol. 2019;70(5):385-391 Authors: Soczomski P, Jurecka-Lubieniecka B, Rogozik N, Tukiendorf A, Jarząb B, Bednarczuk T Abstract INTRODUCTION: Multiple endocrine neoplasia type 1 (MEN1) has been causing problems for clinicians since it was first described in 1954 by Wermer. Not only its rarity, but also its variable clinical manifestations and lack...
Thu Jul 09, 2020 13:40
Related Articles Multifocal mucosa-associated lymphoid tissue lymphoma involving the lungs and the stomach: a rare clinical entity: a case report. Hong Kong Med J. 2019 06;25(3):243-245 Authors: Lam CPM, Wong CF PMID: 31182671 [PubMed - indexed for MEDLINE]
Thu Jul 09, 2020 13:40
Related Articles Role of Adjuvant Multimodality Therapy After Curative-Intent Resection of Ampullary Carcinoma. JAMA Surg. 2019 08 01;154(8):706-714 Authors: Ecker BL, Vollmer CM, Behrman SW, Allegrini V, Aversa J, Ball CG, Barrows CE, Berger AC, Cagigas MN, Christein JD, Dixon E, Fisher WE, Freedman-Weiss M, Guzman-Pruneda F, Hollis RH, House MG, Kent TS, Kowalsky SJ, Malleo G, Salem RR, Salvia R, Schmidt CR, Seykora TF, Zheng R, Zureikat AH, Dickson PV ...
Thu Jul 09, 2020 13:40
Related Articles Disseminated intravascular coagulation and melanoma: a novel case occurring in metastatic melanoma with BRAF and NRAS mutations and systematic review. Melanoma Res. 2019 10;29(5):533-538 Authors: Haggstrom L, Duong TA, Thomas B, Brungs D, Aghmesheh M, Parmar G Abstract Disseminated intravascular coagulation is a complex and potentially lethal complication of malignancy, in which the fundamental abnormality is excessive activation...
Thu Jul 09, 2020 13:40
Related Articles Severe gastrointestinal toxicity of MEK inhibitors. Melanoma Res. 2019 10;29(5):556-559 Authors: Mourad N, Lourenço N, Delyon J, Eftekhari P, Bertheau P, Allayous C, Ballon A, Pagès C, Allez M, Lebbé C, Baroudjian B, PATIO group Abstract Gastrointestinal toxicities of MEK inhibitors in melanoma patients are frequent. In clinical trials, the most common digestive adverse events were nausea, vomiting, and diarrhoea. However,...
Thu Jul 09, 2020 13:40
Related Articles Primary pelvic retroperitoneal ancient schwannoma-a rare diagnosis of pelvic complex cystic lesion. Hong Kong Med J. 2019 04;25(2):160.e1-e3 Authors: Chan TS, Wong T, Pan NY PMID: 30971508 [PubMed - indexed for MEDLINE]
Thu Jul 09, 2020 13:40
Related Articles Immune-related pancreatitis associated with checkpoint blockade in melanoma. Melanoma Res. 2019 10;29(5):549-552 Authors: Kohlmann J, Wagenknecht D, Simon JC, Ziemer M Abstract Recognizing and treating rare checkpoint inhibitor related adverse events may be a clinical challenge in melanoma therapy. One of rather rare affected organs is the pancreas. Immune-related pancreatitis is difficult to recognize due to its variable clinical...
Thu Jul 09, 2020 13:40
Related Articles Incidence of Neoplasia in Pigs and Its Relevance to Clinical Organ Xenotransplantation. Comp Med. 2019 04 01;69(2):86-94 Authors: Jagdale A, Iwase H, Klein EC, Cooper DK Abstract As clinical pig organ xenotransplantation draws closer, more attention is being paid to diseases that affect pigs and those that provide a potential risk to human recipients of pig organs. Neoplasia arising from the pig organ graft is one such concern....
Thu Jul 09, 2020 13:40
Related Articles The Genomic Landscape of Mucinous Breast Cancer. J Natl Cancer Inst. 2019 07 01;111(7):737-741 Authors: Pareja F, Lee JY, Brown DN, Piscuoglio S, Gularte-Mérida R, Selenica P, Da Cruz Paula A, Arunachalam S, Kumar R, Geyer FC, Silveira C, da Silva EM, Li A, Marchiò C, Ng CKY, Mariani O, Fuhrmann L, Wen HY, Norton L, Vincent-Salomon A, Brogi E, Reis-Filho JS, Weigelt B Abstract Mucinous carcinoma of the breast (MCB) is a rare...
Thu Jul 09, 2020 13:40
Related Articles A case report of an intramedullary cervical teratoma in an adult patient with cervical spondylotic radiculopathy. Neurocirugia (Astur). 2019 Sep - Oct;30(5):238-242 Authors: Guadarrama-Ortíz P, Choreño-Parra JA, Carnalla-Cortés M, Sánchez-Garibay C, Palacios-Zúñiga U Abstract Spinal cord teratomas are rare. There are few reports of teratomas affecting the cervical spine and their association with spondylotic radiculopathy has...
Thu Jul 09, 2020 13:40
Related Articles Non-dysraphic intramedullary lipoma of the craniocervical region in an adult: Case report. Neurocirugia (Astur). 2019 Sep - Oct;30(5):250-253 Authors: Iplikcioglu AC, Karabag H Abstract Intradural spinal lipomas with intracranial extension are very rare and are typically diagnosed in childhood. Radical surgical excision usually causes a high rate of morbidity because of the firm adherence between the lipoma and neural tissues....
Thu Jul 09, 2020 13:40
Related Articles A novel surgical technique for aggressive vertebral hemangiomas. Neurocirugia (Astur). 2019 Sep - Oct;30(5):233-237 Authors: Canbay S, Kayalar AE, Gel G, Sabuncuoğlu H Abstract Vertebral hemangiomas are relatively common, but those causing spinal cord compression are rare. A 19-year-old male presented with thoracic back pain. The neurologic examination was normal and radiological examinations demonstrated an aggressive vertebral...
Thu Jul 09, 2020 13:40
Related Articles Concurrent LETM and nerve root enhancement in spinal neurosarcoid: A case series. Mult Scler. 2018 12;24(14):1913-1916 Authors: Deng P, Krasnozhen-Ratush O, William C, Howard J Abstract Spinal neurosarcoidosis is a rare form of neurosarcoid which can be challenging to diagnose given its clinical or radiographic findings are often indistinguishable from other causes of spinal demyelinating disease. We present a series of three...
Thu Jul 09, 2020 13:40
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