Related ArticlesIntraosseous Hibernoma: Five Cases and a Review of the Literature. J Comput Assist Tomogr. 2019 Sep/Oct;43(5):793-798 Authors: Myslicki FA, Rosenberg AE, Chaitowitz I, Subhawong TK Abstract We present 5 cases of intraosseous hibernoma, a rare benign tumor of brown fat. Our literature review reveals that the average age at presentation is 58.6 years, and 69.7% of patients are female. Lesions are most often located in the spine and pelvis....
Related ArticlesCoexistence of phylloides tumour and invasive ductal cancer in the breast. Niger J Clin Pract. 2019 Aug;22(8):1169-1171 Authors: Bozkurt H, Karakaya IB, Aktas E, Irkorucu O Abstract Phylloides tumor in the breast is a rare fibroepithelial tumor, which is often seen in young adult women. Phylloides tumor of the breast accounts for about 1% of all breast tumors and approximately 3% of all fibroepithelial tumors. Pre-operative diagnosis...
Related ArticlesAtypical Location of an Atrial Myxoma: A Case Report. Mymensingh Med J. 2019 Jul;28(3):705-707 Authors: Hossain MA, Vaidya S, Acharya M, Joshi D, Sunny SA, Khan OS Abstract Here, we report a case of a right atrial myxoma attached to the lateral wall, which is seen in only 10% cases, impinging upon the tricuspid valve. A 57 year old male normotensive, non-diabetic, nonsmoker patient was presented to us on 5th of August 2018 with the complaints...
Related ArticlesNodular Mucinosis of Male Breast: A Rare Case Report. Mymensingh Med J. 2019 Jul;28(3):699-704 Authors: Alam F, Joarder AI, Nahid A, Debnath BC, Masud Rana AM, Biswas PK, Khan AS, Jalal MT, Karim SS Abstract Multinodular accumulation of stromal mucin in breast known as nodular mucinosis is an extremely rare condition of breast. Alternatively it is known as myxoma or nerve sheath myxoma of breast. This benign lesion is confined to only...
Related ArticlesGiant Cell Tumour of the Talus: A Rare Case Report. Mymensingh Med J. 2019 Jul;28(3):689-693 Authors: Islam MS, Ara R, Alam MT, Sayed KA, Roy MK, Rahman M, Islam A, Banik SM, Nandi B, Jannat AD, Mohiuddin AM, Sonaullah M Abstract Giant-cell tumor constitutes 4-20% of all primary bone tumors in south East Asian population. They are benign locally aggressive bone tumour first described by cooper in 1818. These tumors occur predominantly...
Related ArticlesBrachial Plexus Schwannoma: A Case Report with Emphasis on Imaging. Mymensingh Med J. 2019 Jul;28(3):685-688 Authors: Ara R, Islam MS, Rashid MH, Khan MN, Chakraborty RK, Rima SZ, Nahar N, Khatun S, Dowel FA, Ara R, Mahmud MA Abstract Brachial plexus tumors are rare. Schwannomas are benign nerve sheath tumors and only about 5% arise from brachial plexus. Diagnosis of these tumors are challenging for radiologists as well as clinicians...
Related ArticlesMesenteric Fibromatosis: A Case Report. Mymensingh Med J. 2019 Jul;28(3):681-684 Authors: Reza E, Nisa AA, Emon RI, Rahman MM, Bhuiyan K Abstract Fibromatosis of mesentery is a very rare disease and only a few cases have been reported. Here we report a case of 40 year old man admitted on 16 October, 2017 in the Department of Surgery (Unit-3) of Mymensingh Medical College Hospital with history of recurrent abdominal pain and progressively...
Related Articles[Suprapubic cartilaginous cyst]. Urologiia. 2019 Jul;(3):122-123 Authors: Pushkar DY, Kasyan GR, Dzhuraeva MD Abstract Suprapubic cartilaginous cyst represents a rare disease. Considering its low prevalence, only 9 clinical case have been described in literature. This lesion is often overlooked due to absence of clinical manifestations, incomplete diagnosis or the lack of necessary information about the disease. We observed a 74-year-old...
Related Articles[Current criteria for the diagnosis of adrenocortical carcinoma]. Arkh Patol. 2019;81(3):66-73 Authors: Selivanova LS, Roslyakova AA, Kovalenko YA, Bogolyubova AV, Tertychnyi AS, Beltsevich DG, Abrosimov AY, Melnichenko GA Abstract Adrenocortical carcinoma is a rare malignant tumor of the adrenal cortex with an unfavorable prognosis. In 2017, the International Agency for Research on Cancer (IARC) and the World Health Organization (WHO)...
Related ArticlesTotal thyroidectomy associated to chemotherapy in primary squamous cell carcinoma of the thyroid. Clin Ter. 2019 Jul-Aug;170(4):e231-e234 Authors: De Cesare A, Di Cristofano C, Di Filippo AR, Salesi N, Spaziani M, Picchio M, Spaziani E Abstract Primary squamous cell carcinoma of the thyroid (PSCCT) is a rare malignant disease with rapid fatal prognosis. The onset is generally characterized by sudden bilateral latero-cervical lymphadenopathy....
Related ArticlesAccurate estimation of cell-type composition from gene expression data. Nat Commun. 2019 07 05;10(1):2975 Authors: Tsoucas D, Dong R, Chen H, Zhu Q, Guo G, Yuan GC Abstract The rapid development of single-cell transcriptomic technologies has helped uncover the cellular heterogeneity within cell populations. However, bulk RNA-seq continues to be the main workhorse for quantifying gene expression levels due to technical simplicity and...
Related ArticlesMalignant Leydig cell tumor in dogs: two cases and a review of the literature. J Vet Diagn Invest. 2019 Jul;31(4):557-561 Authors: Kudo T, Kamiie J, Aihara N, Doi M, Sumi A, Omachi T, Shirota K Abstract Malignant Leydig cell tumor (MLCT) is a rare testicular tumor in dogs. We report herein 2 dogs with MLCT and cutaneous metastasis. Grossly, marked enlargement and distortion of the involved testes were noted; on cut surface, the parenchyma...
Related ArticlesImbalance of Genes Encoding Natural Killer Immunoglobulin-Like Receptors and Human Leukocyte Antigen in Patients With Biliary Cancer. Gastroenterology. 2019 10;157(4):1067-1080.e9 Authors: Cornillet M, Jansson H, Schaffer M, Hertwig L, Berglin L, Zimmer CL, Johansson H, Ellis E, Isaksson B, Gonzalez-Galarza FF, Middleton D, Malmberg KJ, Sparrelid E, Björkström NK Abstract BACKGROUND & AIMS: Bile duct tumors are rare and have poor...
Related ArticlesNeoadjuvant and Adjuvant Treatment with Denosumab in Aggressive Giant-cell Tumor of Bone in the Proximal Fibula: a Case Report. Folia Med (Plovdiv). 2018 Dec 01;60(4):637-640 Authors: Marinova VV, Slavchev SA, Patrikov KD, Tsenova PM, Georgiev GP Abstract Giant cell tumor of bone is a histologically benign but locally aggressive osteolytic lesion, capable of spreading 'benign' metastases mainly to the lungs. Since its description as a...
[Characteristics, diagnosis and treatment of the most common bacterial diseases of the oral cavity].
Related Articles[Characteristics, diagnosis and treatment of the most common bacterial diseases of the oral cavity]. Orv Hetil. 2019 May;160(19):739-746 Authors: Mensch K, Nagy G, Nagy Á, Bródy A Abstract Billions of microorganisms can be found in the oral cavity, from which bacteria are the most frequent. More than 600 bacterial species can be isolated. Most of them are harmless, moreover, some species prove themselves to be specifically useful. However,...
Related Articles[A case of primary leiomyosarcoma originating from the inferior vena cava]. Orv Hetil. 2019 May;160(19):756-761 Authors: Weninger C, Várady E, Omar G, Szabó I, Tornóczky T Abstract The venous invasion from intraabdominal and retroperitoeal tumors (e.g., liver and kidney) is relatively frequent. Primary vascular (venous) tumors are uncommon. The authors review the case of a 67-year-old woman, who was admitted to the hospital in a poor...
Related ArticlesLeyomiomatosis peritonealis disseminata associated with ovarian endometriosis in a patient submitted to hysteroscopic myomectomy. Fertil Steril. 2019 06;111(6):1259-1261 Authors: Mabrouk M, Arena A, Raimondo D, Parisotto M, Caprara G, Seracchioli R Abstract OBJECTIVE: To describe laparoscopic management of a case of leyomiomatosis peritonealis disseminata associated with ovarian endometriosis. DESIGN: Surgical video article....
Related ArticlesBowenoid papulosis unveiling a rare cause of immunosuppression. Int J STD AIDS. 2019 04;30(5):522-525 Authors: Ambooken B, Asokan N, Philip P, Jisha KT Abstract Bowenoid papulosis (BP) is a premalignant condition usually caused by oncogenic types of human papillomavirus (HPV) presenting clinically as warty genital papules. Adult T-cell leukaemia-lymphoma (ATLL) is a peripheral T-cell leukaemia-lymphoma caused by the retrovirus, human...
Related ArticlesGlomus Tumor of the Oral Cavity: Report of a Rare Case and Literature Review. Braz Dent J. 2019 Mar-Apr;30(2):185-190 Authors: Sánchez-Romero C, Oliveira MEP, Castro JFL, Carvalho EJA, Almeida OP, Perez DEDC Abstract Glomus tumor is a benign neoplasm composed of a perivascular proliferation of glomic cells that resembles the normal glomus body. Usually, it appears as a solitary, symptomatic small blue-red nodule, located in the deep...
Related ArticlesEngineering an Artificial T-Cell Stimulating Matrix for Immunotherapy. Adv Mater. 2019 Jun;31(23):e1807359 Authors: Hickey JW, Dong Y, Chung JW, Salathe SF, Pruitt HC, Li X, Chang C, Fraser AK, Bessell CA, Ewald AJ, Gerecht S, Mao HQ, Schneck JP Abstract T cell therapies require the removal and culture of T cells ex vivo to expand several thousand-fold. However, these cells often lose the phenotype and cytotoxic functionality for mediating...
Related ArticlesEpidemiology and Treatment Outcomes of Sinonasal Tumors: A Single Institute's Experience in Pakistan. J Coll Physicians Surg Pak. 2019 Apr;29(4):356-360 Authors: Anjum W, Maken RN, Nisar H, Fatima I, Masood M, Shahid AB Abstract OBJECTIVE: To find the epidemiology and risk factors of sinonasal tumors and treatment outcomes in squamous cell carcinoma. STUDY DESIGN: An observational study. PLACE AND DURATION OF STUDY:...
Related ArticlesA Rare Case of Hypertrophic Gastropathy with Adenocarcinoma Arising from a Gastric-type Adenoma. Intern Med. 2019 Jul 01;58(13):1877-1883 Authors: Kakushima N, Aizawa D, Yoshida M, Ito S, Satoh T, Ono H, Terashima M, Kagawa H, Shimoda T Abstract A 60-year-old man was referred for the investigation of giant gastric folds, life-threatening anemia and hypoproteinemia. A combination of multiple endoscopic procedures derived a clinical diagnosis...
Related ArticlesA 50-Year-Long Study of Waldenström Macroglobulinemia. Mayo Clin Proc. 2019 03;94(3):394-396 Authors: Kastritis E, Dimopoulos MA PMID: 30832789 [PubMed - indexed for MEDLINE]
Related Articles[Mucosal melanoma primary and metastatic cases with urogenital localization in our department]. Orv Hetil. 2019 Mar;160(10):378-385 Authors: Szabó B, Szűcs M, Horváth A, Székely E, Pánczél G, Liszkay G, Holló P, Wikonkál N, Nyirády P Abstract INTRODUCTION: Both primary and metastatic cases of mucosal melanoma in urogenital localization are rare tumors. Only 4-5% of all primary melanomas do not arise from the skin. Extracutaneous melanomas...
Related ArticlesA Rare Case of Negative-Pressure Hydrocephalus: A Plausible Explanation and the Role of Transmantle Theory. World Neurosurg. 2019 05;125:6-9 Authors: Diaz-Romero Paz R, Avendaño Altimira P, Coloma Valverde G, Balhen Martin C Abstract BACKGROUND: Negative-pressure hydrocephalus is a rare condition with the development of symptomatic hydrocephalus despite subnormal intracranial pressure (ICP). The etiology remains unclear. Some authors...
Related ArticlesGiant Thoracic Calcified Disk: Conservative Management with 3-Year Follow-Up. World Neurosurg. 2019 05;125:1-2 Authors: Desai B, Kolcun JPG, Shaffrey ME Abstract Calcified disk herniation of the thoracic spine is by no means a rare clinical entity in neurosurgery. We present a 63-year-old woman with a long-standing giant calcified disk in the thoracic spine. Initial imaging studies indicated a differential diagnosis of calcified disk...
Related ArticlesPrevalence and Clinical Features of Mazabraud Syndrome: A Multicenter European Study. J Bone Joint Surg Am. 2019 Jan 16;101(2):160-168 Authors: Majoor BCJ, van de Sande MAJ, Appelman-Dijkstra NM, Leithner A, Jutte PC, Vélez R, Perlaky T, Staals EL, Bovée JVMG, Hamdy NAT, Dijkstra SPD Abstract BACKGROUND: Mazabraud syndrome is a rare disorder, characterized by the presence of fibrous dysplasia (FD) with associated intramuscular myxomas....
Related ArticlesSpinal Epidural Venous Angioma Presenting Symtomps of Lumbar Disc Herniation: A Case Report. Turk Neurosurg. 2019;29(4):607-610 Authors: Baykara E, Korucu M, Ozdemir M, Gok S Abstract Spinal epidural venous angiomas are extremely rare. We report the case of a 60-year-old man who presented with disc herniation symptoms, complaining of pain in his left leg and numbness, especially at the base of the knee. On physical examination, the Lasègue...
Related ArticlesFamilial Pancreatic Ductal Adenocarcinoma. Am J Pathol. 2019 01;189(1):36-43 Authors: Diaz KE, Lucas AL Abstract Pancreatic ductal adenocarcinoma (PDAC), although a rare disease, has a poor prognosis. With 5-year overall survival of 8%, there is a critical need to detect PDAC early or at a premalignant stage. Current screening methods are largely imaging based, but a more focused screening approach based on modifiable and nonmodifiable...
Related ArticlesDEPArray™ system: An automatic image-based sorter for isolation of pure circulating tumor cells. Cytometry A. 2018 12;93(12):1260-1266 Authors: Di Trapani M, Manaresi N, Medoro G Abstract Circulating tumor cells (CTCs) are rare cells shed into the bloodstream by invasive tumors and their analysis offers a promising noninvasive tool to predict and monitor therapeutic responses. CTCs can be isolated from patient blood and their characterization...
Related ArticlesEvaluation of holographic imaging cytometer holomonitor M4® motility applications. Cytometry A. 2018 11;93(11):1125-1131 Authors: Zhang Y, Judson RL Abstract Digital holographic cytometry (DHC) and other methods of quantitative phase imaging permit extended time-lapse imaging of mammalian cells in the absence of induced cellular toxicity. Manufactured DHC platforms equipped with semi-automated image acquisition, segmentation, and analysis...
Related ArticlesOptic nerve Schwannoma: Neurofibromatosus Type-1? A case report. J Pak Med Assoc. 2018 Jun;68(6):950-952 Authors: Junaid M, Bukhari SS, Rashid MU Abstract Optic nerve Schwannoma is a very rare tumour described in literature. The rarity of this tumour is due to the fact that the optic nerve is myelinated by oligodendrocytes. We present a case of an ancient optic nerve schwannoma in a 16 year old girl who presented to the clinic with right...
Related ArticlesGrowing teratoma syndrome in ovarian germ cell tumours - a diagnostic challenge, two case reports. J Pak Med Assoc. 2018 Jun;68(6):945-946 Authors: Saba A, Khan RS, Ismail H Abstract Growing teratoma syndrome (GTS) is a rare complication of ovarian germ cell tumours and occurs in young age group. It is characterized by clinical or radiological increase in tumour size during or after chemotherapy, with normalization of tumour marker levels....
Related ArticlesChronic myeloid leukaemia presenting as priapism: A case report from Khyber Pakhtunkhwa. J Pak Med Assoc. 2018 Jun;68(6):942-944 Authors: Khan A, Shafiq I, Shah MH, Khan S, Shahid G, Arabdin M Abstract Priapism is known as a very rare complication of leukaemia. We report a 16-years boy who presented with the persistent painful erection of the penis for eleven days. He had aspiration without achieving sustained detumescence. The patient...
A clinicopathologic study on central odontogenic fibroma: with special reference to amyloid variant.
Related ArticlesA clinicopathologic study on central odontogenic fibroma: with special reference to amyloid variant. Oral Surg Oral Med Oral Pathol Oral Radiol. 2018 Dec;126(6):513-520 Authors: Zhou CX, Li TJ Abstract OBJECTIVE: The aim of this study was to clarify the clinicopathologic features of central odontogenic fibroma (OF), especially the amyloid variant, and to discuss its association with the Langerhans cell variant of calcifying epithelial...
Related ArticlesThe RareCyte® platform for next-generation analysis of circulating tumor cells. Cytometry A. 2018 12;93(12):1220-1225 Authors: Kaldjian EP, Ramirez AB, Sun Y, Campton DE, Werbin JL, Varshavskaya P, Quarre S, George T, Madan A, Blau CA, Seubert R Abstract Circulating tumor cells (CTCs) can reliably be identified in cancer patients and are associated with clinical outcome. Next-generation "liquid biopsy" technologies will expand CTC diagnostic...
Related ArticlesCD5 positive B-ALL, a uniquely aggressive subcategory of B-ALL? A case report and brief review of the literature. Pediatr Blood Cancer. 2019 01;66(1):e27484 Authors: Staley EM, Feldman AZ, Koenig RG, Hill B Abstract CD5 antigen expression in B-cell acute lymphoblastic leukemia (B-ALL) is exceptionally rare. There are six detailed case reports in the literature, with only 16 cases described. Case series analyzing the frequency of aberrant...
Related ArticlesPeripheral blood flow cytometry for the diagnosis of pediatric acute leukemia: Highly reliable with rare exceptions. Pediatr Blood Cancer. 2019 01;66(1):e27453 Authors: Cheng J, Klairmont MM, Choi JK Abstract BACKGROUND: Recent data have demonstrated the high sensitivity and specificity of peripheral blood flow cytometry (PBFC) for the diagnosis of pediatric leukemia; however, diagnostically significant immunophenotypic discrepancies...
Related ArticlesFatal Toxic Effects Associated With Immune Checkpoint Inhibitors: A Systematic Review and Meta-analysis. JAMA Oncol. 2018 12 01;4(12):1721-1728 Authors: Wang DY, Salem JE, Cohen JV, Chandra S, Menzer C, Ye F, Zhao S, Das S, Beckermann KE, Ha L, Rathmell WK, Ancell KK, Balko JM, Bowman C, Davis EJ, Chism DD, Horn L, Long GV, Carlino MS, Lebrun-Vignes B, Eroglu Z, Hassel JC, Menzies AM, Sosman JA, Sullivan RJ, Moslehi JJ, Johnson DB Abstract ...
Related ArticlesCrizotinib-Induced Fulminant Hepatic Failure: A Rare Adverse Event. J Glob Oncol. 2018 09;4:1-4 Authors: Adhikari N, Kumar P, Venkatesulu BP, Pandey R, Haresh KP, Gupta S, Sharma DN, Rath GK PMID: 30241172 [PubMed - indexed for MEDLINE]
Related ArticlesCharacterization of long-term outcomes for pediatric patients with epithelioid hemangioma. Pediatr Blood Cancer. 2019 01;66(1):e27451 Authors: Liu KX, Duggan EM, Al-Ibraheemi A, Shaikh R, Adams DM Abstract Epithelioid hemangioma (EH) is a rare benign vascular tumor that occurs in soft tissues and bone and presents between the third and sixth decades of life. Little is known about the clinical course and outcomes of pediatric EH. We report...
Related ArticlesOutcome of Wilms tumor patients with bone metastasis enrolled on National Wilms Tumor Studies 1-5: A report from the Children's Oncology Group. Pediatr Blood Cancer. 2019 01;66(1):e27430 Authors: Iaboni DSM, Chi YY, Kim Y, Dome JS, Fernandez CV Abstract BACKGROUND: Wilms tumor (WT) is the most common renal tumor in children. We describe the outcomes for patients with WT that metastasized to bone (WTBM) to assist in decision making for...
Related ArticlesAnal squamous cell carcinoma: are we improving outcomes? ANZ J Surg. 2018 10;88(10):1013-1016 Authors: Mackowski A, Levitt M, Makin G, Salama P, Tan P, Penter C, Platell C Abstract BACKGROUND: Anal squamous cell carcinoma (SCC) is a rare malignancy. The purpose of this study was to review a single institution's experience. METHODS: All patients with anal SCC from St John of God Subiaco Hospital database were identified over...
Related ArticlesExploration of BRAFV600E as a diagnostic adjuvant in the non-invasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP). Hum Pathol. 2018 12;82:32-38 Authors: Johnson DN, Sadow PM Abstract The non-invasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP) and encapsulated follicular variant of papillary thyroid carcinoma (EFVPTC) are distinguished from classical papillary thyroid carcinoma...
Related ArticlesThe Parsortix™ Cell Separation System-A versatile liquid biopsy platform. Cytometry A. 2018 12;93(12):1234-1239 Authors: Miller MC, Robinson PS, Wagner C, O'Shannessy DJ Abstract Cancer cells from solid tumors can enter the circulatory system and survive to subsequently form distant metastases. The CellSearch® system (Menarini-Silicon Biosystems, Huntingdon Valley, PA) was the first, FDA-cleared system that provided a reliable tool...
Related ArticlesClinicopathologic Features and Clinical Outcome Differences in De Novo Versus Secondary Histiocytic Sarcomas: A Multi-institutional Experience and Review of the Literature. Clin Lymphoma Myeloma Leuk. 2018 10;18(10):e427-e435 Authors: Broadwater DR, Conant JL, Czuchlewski DR, Hall JM, Wei S, Siegal GP, Peker D Abstract INTRODUCTION: Histiocytic sarcoma (HS) is a rare malignant neoplasm that can occur in patients with a history of treatment...
Related ArticlesPositron Emission Tomography-based Analysis Can Accurately Predict Bone Marrow Involvement With Mantle Cell Lymphoma. Clin Lymphoma Myeloma Leuk. 2018 11;18(11):731-736 Authors: Morgan R, Perry M, Kwak J, Jensen A, Kamdar M Abstract INTRODUCTION: Mantle cell lymphoma (MCL) is a rare subtype of non-Hodgkin lymphoma and requires both bone marrow biopsy and fluorine-18 fluorodeoxyglucose (FDG) positron emission tomography/computed tomography...
Related ArticlesFamilial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family. Sci Rep. 2018 08 02;8(1):11635 Authors: Kumar A, Bandapalli OR, Paramasivam N, Giangiobbe S, Diquigiovanni C, Bonora E, Eils R, Schlesner M, Hemminki K, Försti A Abstract Whole-genome sequencing methods in familial cancer are useful to unravel rare clinically important cancer predisposing variants. Here, we present improvements...
Related ArticlesDefining the frequency of human papillomavirus and polyomavirus infection in urothelial bladder tumours. Sci Rep. 2018 07 26;8(1):11290 Authors: Llewellyn MA, Gordon NS, Abbotts B, James ND, Zeegers MP, Cheng KK, Macdonald A, Roberts S, Parish JL, Ward DG, Bryan RT Abstract Given the contradictory nature of the literature regarding the role of human papillomaviruses and polyomaviruses in the pathogenesis of urothelial bladder cancer...
Related ArticlesPD-1, PD-L1, and CD163 in pancreatic undifferentiated carcinoma with osteoclast-like giant cells: expression patterns and clinical implications. Hum Pathol. 2018 11;81:157-165 Authors: Luchini C, Cros J, Pea A, Pilati C, Veronese N, Rusev B, Capelli P, Mafficini A, Nottegar A, Brosens LAA, Noë M, Offerhaus GJA, Chianchiano P, Riva G, Piccoli P, Parolini C, Malleo G, Lawlor RT, Corbo V, Sperandio N, Barbareschi M, Fassan M, Cheng L, Wood LD, Scarpa A ...
Related ArticlesRoles of human epidermal growth factor receptor family in pulmonary lymphangioleiomyomatosis. Hum Pathol. 2018 11;81:121-130 Authors: Kobayashi K, Miki Y, Saito R, Adachi K, Seyama K, Okada Y, Sasano H Abstract Lymphangioleiomyomatosis (LAM) is a rare and refractory disease that affects women of reproductive age. Several target therapies are used to manage LAM, but no curative modes of treatment have been reported yet. Therefore, in...
Related ArticlesBiallelic tumour suppressor loss and DNA repair defects in de novo small-cell prostate carcinoma. J Pathol. 2018 10;246(2):244-253 Authors: Chedgy EC, Vandekerkhove G, Herberts C, Annala M, Donoghue AJ, Sigouros M, Ritch E, Struss W, Konomura S, Liew J, Parimi S, Vergidis J, Hurtado-Coll A, Sboner A, Fazli L, Beltran H, Chi KN, Wyatt AW Abstract Small-cell prostate carcinoma (SCPC) is an aggressive malignancy that is managed similarly...
Related ArticlesRole of Immunotherapy in the Treatment of Squamous Cell Carcinoma of the Anal Canal. J Natl Compr Canc Netw. 2018 07;16(7):903-908 Authors: Morris VK, Eng C Abstract Anal cancer is a rare malignancy for which cisplatin with 5-fluorouracil is the recommended treatment for patients with metastatic disease. Because most cases of anal cancer are linked to prior infection with oncogenic strands of the human papillomavirus, immunotherapeutic...
Related ArticlesShunt Dependency Syndrome after Cyst-Peritoneal Shunt Resolved by Keyhole Microsurgical Cyst Resection: Two Case Reports and Literature Review. Neuropediatrics. 2018 10;49(5):310-313 Authors: Dong F, Wang Z, Li Y, Chen Z, Zhang S, Wan F Abstract OBJECTIVE: Shunt dependency syndrome after cyst-peritoneal (CP) shunt is a rare but serious complication which leads to increased intracranial pressure and neurological deficit. The possible...
Related ArticlesPrognostic Significance of BCL-2 and BCL-6 Expression in MYC-positive DLBCL. Clin Lymphoma Myeloma Leuk. 2018 10;18(10):e381-e389 Authors: Li L, Zhang X, Zhang T, Song Z, Hu G, Li W, Li L, Qiu L, Qian Z, Zhou S, Liu X, Feng L, Pan Y, Zhai Q, Meng B, Ren X, Fu K, Wang P, Wang X, Zhang H Abstract BACKGROUND: Double-expression lymphoma (DEL) is a rare subgroup of diffuse large B-cell lymphoma (DLBCL), which has coexpression of MYC and BCL-2....
Related ArticlesA patient with polycystic kidney disease, hepatic cysts and atrial myxoma. Saudi J Kidney Dis Transpl. 2018 May-Jun;29(3):723-727 Authors: Alfishawy M, Ali H, Daoud A Abstract With the development of renal replacement therapy, cardiovascular complications have become the major cause of death in patients with polycystic kidney disease (PKD). Atrial myxoma is a cardiac abnormality that has been rarely reported with PKD. The presence of...
Related ArticlesAcquired haemophilia A imitating uterine tumour in a patient with de novo diagnosis of hepatitis C. Anaesthesiol Intensive Ther. 2018;50(2):170-172 Authors: Czempik PF, Krzych ŁJ Abstract AHA is an extremely rare disorder, with annual incidence of 1.5 cases per million population. This clinical entity is caused by autoantibodies directed against coagulation factor VIII, what leads to decreased serum activity of thereof, and is characterized...
Related ArticlesMixed-phenotype large granular lymphocytic leukemia: a rare subtype in the large granular lymphocytic leukemia spectrum. Hum Pathol. 2018 11;81:96-104 Authors: Neff JL, Rangan A, Jevremovic D, Nguyen PL, Chiu A, Go RS, Chen D, Morice WG, Shi M Abstract Large granular lymphocytic leukemia (LGLL) is a chronic proliferation of cytotoxic lymphocytes in which more than 70% of patients develop cytopenia(s) requiring therapy. LGLL includes...
Related ArticlesGlomeruloid hemangioma associated with TAFRO syndrome. Hum Pathol. 2018 12;82:172-176 Authors: Shinozaki-Ushiku A, Higashihara T, Ikemura M, Sato J, Nangaku M, Ushiku T, Fukayama M Abstract Glomeruloid hemangioma is a rare cutaneous lesion that has been considered as a specific cutaneous marker of POEMS syndrome. Herein, we present the first case of glomeruloid hemangioma associated with TAFRO syndrome, a unique variant of idiopathic...
Δεν υπάρχουν σχόλια:
Δημοσίευση σχολίου