Related Articles[A Case of Meningeal Solitary Fibrous Tumour/Haemangiopericytoma WHO Grade III Metastasized to the Spleen Shortly After Tumor Resection]. No Shinkei Geka. 2019 Mar;47(3):329-334 Authors: Enomoto T, Aoki M, Kobayashi H, Abe H, Ishii F, Yamauchi Y, Inoue T, Nabeshima K Abstract Revision of WHO guidelines in 2016 led to the classification of solitary fibrous tumours(SFTs)and haemangiopericytomas(HPCs)as a single tumor entity characterized...
Related ArticlesThermal injury to spinal cord, a rare complication of percutaneous microwave spine tumor ablation: Case report. J Clin Neurosci. 2019 Jun;64:50-54 Authors: Westbroek EM, Goodwin ML, Hui F, Khan MA, Sciubba DM Abstract Metastatic disease to the spine are becoming increasingly common with an aging population and improvements in systemic cancer therapies. Surgery, radiation, and vertebroplasty are mainstay modalities for treating painful...
Related ArticlesDiffuse spinal spreading following previous intracranial intradural chordoma resection: A rare case report. J Clin Neurosci. 2019 Jun;64:44-46 Authors: Vellutini EAS, Brock RS, Martins HO, Taricco MA, de Oliveira MF Abstract INTRODUCTION: Chordoma is a malignant tumor that usually involves the axial skeleton. Intradural chordomas are even rarer and 37 cases have been reported to the best of our knowledge. We present a case of a patient...
Related ArticlesMalignant perivascular epithelioid cell tumor of the lung synchronous with a primary adenocarcinoma: one case report and review of the literature. BMC Cancer. 2019 Mar 15;19(1):235 Authors: Zhao J, Teng H, Zhao R, Ding W, Yu K, Zhu L, Zhang J, Han Y Abstract BACKGROUND: Perivascular Epithelioid Cell Tumors (PEComa) is an extraordinarily rare mesenchymal neoplasm especially the malignant type originating from the lung. To date, only...
Related ArticlesAneurysmal Fibrous Histiocytoma: Clinicopathology Analysis of 30 Cases of a Rare Variant of Cutaneous Fibrohistiocytoma. Curr Med Sci. 2019 Feb;39(1):134-137 Authors: Nabatanzi A, Male M, Qu XY, Li YQ, Meng X, Di WS, Huang CZ Abstract Aneurysmal fibrous histiocytoma is often clinically misdiagnosed. In this study, we put forward an insight on how to help diagnose this disease clinically. A retrospective chart review was performed on...
Related ArticlesComplications from percutaneous microwave ablation of liver tumours: a pictorial review. Br J Radiol. 2019 Jul;92(1099):20180864 Authors: Fang C, Cortis K, Yusuf GT, Gregory S, Lewis D, Kane P, Peddu P Abstract Percutaneous microwave ablation of liver tumours is a well-established technique that has been proven to be effective in the curative and palliative treatment of small volume primary and secondary liver tumours. Microwave ablation...
Related ArticlesRare-Earth-Doped Calcium Carbonate Exposed to X-ray Irradiation to Induce Reactive Oxygen Species for Tumor Treatment. Int J Mol Sci. 2019 03 06;20(5): Authors: Yang CC, Wang WY, Lin FH, Hou CH Abstract Conventional photodynamic therapy (PDT) is limited by its penetration depth due to the photosensitizer and light source. In this study, we developed X-ray induced photodynamic therapy that applied X-ray as the light source to activate...
Related ArticlesDiagnosis and treatment complications of primary cardiac lymphoma in an immunocompetent 28-year old man: a case report. BMC Cancer. 2019 Mar 01;19(1):191 Authors: Bonou M, Kapelios CJ, Marinakos A, Adamopoulos S, Diamantopoulos P, Foukas PG, Kaklamanis L, Korkolopoulou P, Barbetseas J, Viniou NA Abstract BACKGROUND: Primary cardiac lymphomas (PCL) represent extremely rare cardiac tumors which are accompanied by poor prognosis, unless...
Related ArticlesPrimary Squamous Cell Carcinoma in the Thyroid Gland: A Population-Based Analysis Using the SEER Database. World J Surg. 2019 05;43(5):1249-1255 Authors: Yang S, Li C, Shi X, Ma B, Xu W, Jiang H, Liu W, Ji Q, Wang Y Abstract OBJECTS: To evaluate prognostic factors and treatment outcomes of primary squamous cell carcinoma in thyroid (PSCCTh) over the past decades using a large national database. METHODS: All patients diagnosed...
Related ArticlesGastric Cancer, Hemophilia A and Angiodysplasia - An Unreported Association with Clinical Implications in a Patient with Digestive Hemorrhage. Chirurgia (Bucur). 2018 Nov-Dec;113(6):857-866 Authors: Martiniuc A, Grasu M, Dumitru R, Toma M, Rusu G, Manga G, Scărlătescu E, Cotruţă B, Brâză M, Stoia R, Herlea V, Dumitraşcu T Abstract Introduction: Gastric cancer is a rare cause of upper digestive hemorrhage. Associated co-morbidities may...
Related ArticlesOrthotopic Liver Transplantation for Hereditary Hemorrhagic Telangiectasia and MEN Type I Syndrome - Case Report and Review of Literature. Chirurgia (Bucur). 2018 Nov-Dec;113(6):837-848 Authors: Ionescu MI, Edwin ID, Wilson CH, Saikia SE, Talbot D Abstract Introduction: Hereditary haemorrhagic telangiectasia (HHT) is a rare autosomal dominant genetic disorder characterized by arteriovenous malformations (AVMs) mainly affecting the lungs...
Related ArticlesTransplantation. Cancer Treat Res. 2019;176:269-287 Authors: Zain J Abstract Mature T-cell non-Hodgkin lymphomas (T-cell NHL) are a heterogeneous group of lymphoid malignancies including NK/T-cell lymphomas. Hematopoietic cell transplantation (HCT) is an important component of the management of T-cell NHL; however, the optimal timing and type of transplant for each different subtype is an ongoing debate. For the purpose of this chapter,...
Related ArticlesRare T-Cell Subtypes. Cancer Treat Res. 2019;176:195-224 Authors: van der Weyden C, McCormack C, Lade S, Johnstone RW, Prince HM Abstract There are a number of rare T-cell lymphoma subtypes that may be encountered in clinical practice. In recent years, improved immunohistochemical techniques and molecular tumor profiling have permitted refinement of some of the diagnostic categories in this group, as well as the recognition of distinct...
Related ArticlesHepatosplenic T-Cell Lymphomas. Cancer Treat Res. 2019;176:185-193 Authors: Gowda L, Foss F Abstract Hepatosplenic T-cell lymphoma (HSTL) is a rare variant of extranodal peripheral T-cell lymphomas (PTCL), associated with aggressive disease course and a relentless track record for lethal outcomes. HSTL presents commonly in young men in their third or fourth decade. Of the known causes, immune dysregulation and immunosuppression are the...
Related ArticlesNK-Cell Lymphomas. Cancer Treat Res. 2019;176:163-184 Authors: Chihara D, Oki Y Abstract NK-cell malignancies are rare aggressive diseases associated with poor clinical outcome. There is a significant geographic variation in their incidence. At least a part of the reason for that is the fact that Epstein-Barr virus plays an important role in pathogenesis, and importantly, the plasma viral titer reflects disease burden and response to...
Related ArticlesEpidemiology and Pathology of T- and NK-Cell Lymphomas. Cancer Treat Res. 2019;176:1-29 Authors: Siaghani PJ, Wong JT, Chan J, Weisenburger DD, Song JY Abstract PURPOSE: This review will describe and update readers on the recent changes in the 2017 WHO classification regarding peripheral T-cell lymphomas. RECENT FINDINGS: Signficant advances in molecular studies have resulted in revisions to the classification as well as introduction...
Related Articles[Clinical and laboratory characteristics of hematopathy with t(5;12)(q33;p13) translocation]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Dec 10;35(6):879-882 Authors: Wang S, Li L, Wang J Abstract OBJECTIVE: To investigate the clinical and laboratory characteristics of hematopoietic tumor with t(5;12)(q33;p13). To sum up the similarities and differences of these diseases. METHODS: The chromosome samples were prepared by short-term...
Related Articles[Hybrid prosthesis for vascular reconstruction of the internal carotid artery near the skull base after radical excision of a very rare malignant glomus caroticum paraganglioma]. HNO. 2019 Mar;67(3):207-211 Authors: Arens C, Granowski D, Udelnow A, Meyer F, Jechorek D, Halloul Z Abstract BACKGROUND: Neck tumors are challenging regarding the diagnostic and therapeutic management particularly in cases of malignant growth near relevant...
Related ArticlesA clinical analysis of 114 cases of sarcomatoid carcinoma of the lung. Clin Exp Med. 2018 Nov;18(4):555-562 Authors: Hou J, Xing L, Yuan Y Abstract The aim was to investigate the clinicopathological characteristics, diagnosis, and prognosis of sarcomatoid carcinoma of the lung. We reviewed 114 cases of sarcomatoid carcinoma of the lung in patients that were admitted to the First Affiliated Hospital of Zhengzhou University and Anyang...
Related ArticlesA unique model for SDH-deficient GIST: an endocrine-related cancer. Endocr Relat Cancer. 2018 11;25(11):943-954 Authors: Powers JF, Cochran B, Baleja JD, Sikes HD, Zhang X, Lomakin I, Langford T, Stein KT, Tischler AS Abstract We describe a unique patient-derived xenograft (PDX) and cell culture model of succinate dehydrogenase-deficient gastrointestinal stromal tumor (SDH-deficient GIST), a rare mesenchymal tumor that can occur in association...
Related ArticlesParathyroid carcinoma in multiple endocrine neoplasm type 1 syndrome: case report and systematic literature review. Clin Exp Med. 2018 Nov;18(4):585-593 Authors: Di Meo G, Sgaramella LI, Ferraro V, Prete FP, Gurrado A, Testini M Abstract The aim of this report was to illustrate a case of parathyroid carcinoma (PC) in a patient with multiple endocrine neoplasia type 1 (MEN1) along with a comprehensive literature review. A 61-year-old...
Related ArticlesRapid proteomic analysis for solid tumors reveals LSD1 as a drug target in an end-stage cancer patient. Mol Oncol. 2018 08;12(8):1296-1307 Authors: Doll S, Kriegmair MC, Santos A, Wierer M, Coscia F, Neil HM, Porubsky S, Geyer PE, Mund A, Nuhn P, Mann M Abstract Recent advances in mass spectrometry (MS)-based technologies are now set to transform translational cancer proteomics from an idea to a practice. Here, we present a robust proteomic...
Related ArticlesSurvival Outcomes Associated With Female Primary Urethral Carcinoma: Review of a Single Institutional Experience. Clin Genitourin Cancer. 2018 10;16(5):e1003-e1013 Authors: Peyton CC, Azizi M, Chipollini J, Ercole C, Fishman M, Gilbert SM, Juwono T, Lockhart J, Poch M, Pow-Sang JM, Spiess PE, Wiegand L, Sexton WJ Abstract BACKGROUND: Primary urethral carcinoma (PUC) is rare, and standard treatment recommendations are lacking. We examined...
Related ArticlesThe Comparing Options for Management: PAtient-centered REsults for Uterine Fibroids (COMPARE-UF) registry: rationale and design. Am J Obstet Gynecol. 2018 07;219(1):95.e1-95.e10 Authors: Stewart EA, Lytle BL, Thomas L, Wegienka GR, Jacoby V, Diamond MP, Nicholson WK, Anchan RM, Venable S, Wallace K, Marsh EE, Maxwell GL, Borah BJ, Catherino WH, Myers ER Abstract BACKGROUND: Uterine fibroids are common in premenopausal women, yet comparative...
Related ArticlesExome chip analyses identify genes affecting mortality after HLA-matched unrelated-donor blood and marrow transplantation. Blood. 2018 05 31;131(22):2490-2499 Authors: Zhu Q, Yan L, Liu Q, Zhang C, Wei L, Hu Q, Preus L, Clay-Gilmour AI, Onel K, Stram DO, Pooler L, Sheng X, Haiman CA, Zhu X, Spellman SR, Pasquini M, McCarthy PL, Liu S, Hahn T, Sucheston-Campbell LE Abstract Although survival outcomes have significantly improved, up to...
Related ArticlesIsolated Optic Nerve Glioma in Children With and Without Neurofibromatosis: Retrospective Characterization and Analysis of Outcomes. J Child Neurol. 2018 05;33(6):375-382 Authors: Hamideh D, Hoehn ME, Harreld JH, Klimo PD, Gajjar A, Qaddoumi I Abstract Isolated optic nerve glioma is a rare tumor with no consensus for the best therapeutic approach. Therefore, tumor control and preservation of visual function remain a challenge. In this...
Related ArticlesGenetic alterations and tumor immune attack in Yo paraneoplastic cerebellar degeneration. Acta Neuropathol. 2018 04;135(4):569-579 Authors: Small M, Treilleux I, Couillault C, Pissaloux D, Picard G, Paindavoine S, Attignon V, Wang Q, Rogemond V, Lay S, Ray-Coquard I, Pfisterer J, Joly F, Du Bois A, Psimaras D, Bendriss-Vermare N, Caux C, Dubois B, Honnorat J, Desestret V Abstract Paraneoplastic cerebellar degenerations with anti-Yo antibodies...
Related ArticlesNanozyme Decorated Metal-Organic Frameworks for Enhanced Photodynamic Therapy. ACS Nano. 2018 01 23;12(1):651-661 Authors: Zhang Y, Wang F, Liu C, Wang Z, Kang L, Huang Y, Dong K, Ren J, Qu X Abstract Metal-organic frameworks (MOFs) have been used for photodynamic therapy (PDT) of cancers by integrating photosensitizers, which cause cytotoxic effects on cancer cells by converting tumor oxygen into reactive singlet oxygen (1O2). However,...
Related ArticlesRadiation-induced spinal nerve root cavernous malformations as a rare cause of radiculopathy. Neurology. 2017 11 28;89(22):2299-2300 Authors: Rastogi K, Klein CJ, O'Toole JE, Jhaveri MD, Malik R PMID: 29180575 [PubMed - indexed for MEDLINE]
Related ArticlesCompressive Ulnar Neuropathy Caused by Olecranon Bursitis and Concomitant Epidermal Cyst: A Case Report. J Hand Surg Asian Pac Vol. 2017 Dec;22(4):503-507 Authors: Yamazaki H, Shinone M, Kato H Abstract Epidermal cyst is a dermal or subcutaneous epithelial cyst that contains keratin and is lined by true epidermis. Although extremely rare, it can cause pathology including nerve compression syndrome. We report a rare case of ulnar nerve...
Related ArticlesAncient Schwannoma of Radial Nerve: A Report of Two Cases. J Hand Surg Asian Pac Vol. 2017 Dec;22(4):526-530 Authors: Bhat AK, Acharya AM, Narayanakurup JK, Shankar V Abstract Ancient schwannoma is a rare variant of schwannoma associated with a longstanding course. They differ from classical schwannomas in the long duration for this subtype of schwannoma to develop and also by demonstrating haemorrhagic and degenerative changes with nuclear...
Related ArticlesThe autophagy scaffold protein ALFY is critical for the granulocytic differentiation of AML cells. Sci Rep. 2017 10 11;7(1):12980 Authors: Schläfli AM, Isakson P, Garattini E, Simonsen A, Tschan MP Abstract Acute myeloid leukemia (AML) is a malignancy of myeloid progenitor cells that are blocked in differentiation. Acute promyelocytic leukemia (APL) is a rare form of AML, which generally presents with a t(15;17) translocation causing...
Related ArticlesGiant Mediastinal Thymic Cyst. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2017 Sep 01;38(2):139-145 Authors: Kondov G, Kondov B, Srceva MJ, Damjanovski G, Ferati I, Karapetrov I, Topuzovska IK, Tanevska N, Kokareva A Abstract The authors present a rare case of giant mediastinal cyst which arises from the thymus gland, and goes down in both pleural spaces, especially in the right chest cavity where a dominant part of the cyst was present....
Related ArticlesA rare giant chronic polypoidal endocervicits in a premenopausal woman; case report. Eur J Obstet Gynecol Reprod Biol. 2017 11;218:137-138 Authors: Shaamash AH, Abbas AM, Badary DM PMID: 28882461 [PubMed - indexed for MEDLINE]
Related ArticlesParathyroid adenoma with concurrent toxic thyroid adenoma: a rare combination. S Afr J Surg. 2017 Mar;55(1):41-44 Authors: Sardiwalla II, Mokhtari A, Sardiwalla Y Abstract BACKGROUND: Hypercalcemia in association with hyperthyroidism is a well-recognized phenomenon. Primary hyperparathyroidism due to parathyroid adenoma in association with thyroid adenoma is extremely rare. These cases can present a diagnostic and therapeutic challenge...
Related ArticlesBreast ductal carcinoma in situ in an unscreened population: presentation, diagnosis and management at a single tertiary centre. S Afr J Surg. 2017 Mar;55(1):4-9 Authors: Mutebi M, Simonds H Abstract BACKGROUND: To determine the clinical presentation of patients presenting with isolated ductal carcinoma in situ at a single tertiary center in the Cape Town, South Africa. To review the diagnostic techniques most commonly used and the primary...
Related ArticlesDorsal Wrist Ganglion Associated with Extensor Digitorum Brevis Manus: Case Report and Review of the Literature. J Hand Surg Asian Pac Vol. 2017 Sep;22(3):355-358 Authors: Feintisch AM, Datiashvili R Abstract Aberrant accessory muscles are rare entities in the hand. The extensor digitorum brevis manus (EDBM) muscle is amongst them and may be seen in association with dorsal ganglion cysts. Distinguishing an EDBM muscle is relevant in the...
Related ArticlesPrimary intracranial leiomyoma in renal transplant recipient. Saudi J Kidney Dis Transpl. 2017 Jul-Aug;28(4):921-924 Authors: Patel U, Patel N Abstract Leiomyoma, the benign tumor of smooth muscle cell origin, is commonly seen in genitourinary and gastrointestinal tracts. Primary intracranial leiomyoma, however, is extremely rare occurrence. We hereby report a case of Epstein-Barr negative primary intracranial leiomyoma in a middle-aged...
Related ArticlesA rare case of a lipoma of the cranio-cervical junction in a middle-aged patient. J Neurosurg Sci. 2017 Oct;61(5):551-554 Authors: Zollino G, Vitali M, Grasso V, Bertuccio A, Longo GP, Barbanera A PMID: 28737367 [PubMed - indexed for MEDLINE]
Related ArticlesAn atypical type I gastric neuroendocrine tumor. Rom J Intern Med. 2017 Dec 01;55(4):253-256 Authors: Gheorghe AV, Rimbas M, Ginghina O, Spanu A, Voiosu TA Abstract BACKGROUND: Gastric neuroendocrine tumors (GI-NETs) are rare lesions, usually discovered incidentally during endoscopy. Based on their pathology, there are 4 types of GI-NETs. Type I are multiple small polypoid lesions with central ulceration located in the gastric body or...
Related ArticlesCalvarial Ewing's sarcoma, a rare childhood tumor: Report and a review of literature. Neurol India. 2017 Jul-Aug;65(4):904-906 Authors: Nair P, Aggarwal V, Kumar K, Mathews A, Abraham M, Nair S PMID: 28681782 [PubMed - indexed for MEDLINE]
Related ArticlesPediatric cemento-ossifying fibroma of the orbital roof: Rare pathology at a rare location. Neurol India. 2017 Jul-Aug;65(4):902-903 Authors: Verma SK, Garg K, Tandon V, Kumari K, Sharma MC, Kale SS, Sharma BS PMID: 28681781 [PubMed - indexed for MEDLINE]
Related ArticlesLumbar extradural arteriovenous malformation mimicking a schwannoma in a child: Rare presentation of neurofibromatosis type-1. Neurol India. 2017 Jul-Aug;65(4):900-902 Authors: Jonathan GE, Nair BR, Joseph V, Mani S, Chacko G PMID: 28681780 [PubMed - indexed for MEDLINE]
Related ArticlesSolitary primary leptomeningeal astrocytoma - An extremely rare pathology. Neurol India. 2017 Jul-Aug;65(4):898-900 Authors: Sharma R, Garg K, Rajeshwari M, Sharma MC, Kale SS PMID: 28681779 [PubMed - indexed for MEDLINE]
Related ArticlesA rare primary cardiac benign tumour: diagnosis by non-invasive cardiac imaging. Acta Cardiol. 2017 Jun;72(3):345-346 Authors: Godinho AR, Dias P, Almeida PB, Pinho T, Maciel MJ PMID: 28636516 [PubMed - indexed for MEDLINE]
Related ArticlesExtremely Locally Advanced Ovarian Malignant Mixed Mullerian Tumor in 37-Years-Old Female. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2017 Mar 01;38(1):75-79 Authors: Jota G, Gelevski R, Karadzov Z, Selmani R, Genadieva-Dimitrova M, Peneva M, Jovanovska-Manevska V Abstract Ovarian carcinosarcomas, rare variant of ovarian carcinoma, composed of both carcinomatous and mesenchymal components, solid and/or cystic, fleshy and hemorrhagic,...
Related ArticlesCecal carcinoid tumor in a nigerian man: A case report and review of literature. Niger J Clin Pract. 2017 05;20(5):634-636 Authors: Obateru OA, Taiwo JA, Oladejo S, Awelimobor DA, Fadaunsi OO, Olokoba AB Abstract Carcinoid tumors are rare neuroendocrine tumors that have been reported in a wide range of organs but most commonly involve the gastrointestinal tract (stomach, ileum, appendix, and colon), and rarely ovary and thymus. We present...
Related ArticlesMetastasis of Renal Cell Carcinoma to the Trapezium. J Hand Surg Asian Pac Vol. 2017 Jun;22(2):262-265 Authors: Nakagawa R, Susa M, Nakayama R, Watanabe I, Horiuchi K, Toyama Y, Nakamura M, Matsumoto M, Morioka H Abstract Solitary metastasis of a carcinoma to carpal bone is extremely rare. Metastases of renal cell carcinoma (RCC) usually occur in a multiple fashion and there has been no report to date of a solitary metastasis to trapezium...
Related ArticlesOsteoid Osteoma of the Distal Phalanx of the Ring Finger with Clubbed Finger Deformity: A Case Report. J Hand Surg Asian Pac Vol. 2017 Jun;22(2):248-250 Authors: Horiuchi K, Horiuchi Y, Ochi K Abstract Osteoid osteoma of the distal phalanx is very rare. We describe a case of osteoid osteoma of the distal phalanx of the ring finger with clubbed finger deformity that improved after tumour removal. A 50-year-old left-handed man presented...
Related ArticlesPainful Snapping of Thumb Caused by Osteochondroma of Trapezium. J Hand Surg Asian Pac Vol. 2017 Jun;22(2):255-258 Authors: Anantavorasakul N, Uerpairojkit C, Leechavengvongs S Abstract Osteochondroma is the most common benign bone tumor. Lesions occurring at the carpal bones are extremely rare. There are very few cases of osteochondroma at the trapezium had been reported in the English literature. We reported a 47-year-old patient with...
Related ArticlesPacinian Corpuscles Neuroma. An Exceptional Cause of Pain in the Hand. J Hand Surg Asian Pac Vol. 2017 Jun;22(2):229-231 Authors: Jiménez I, Marcos-García A, Muratore G, Medina J Abstract Pacinian corpuscles are rapidly adapting mechanoreceptors mainly distributed in the dermis of the fingers and palm of the hand. A neuroma of the Pacinian corpuscle is a rare and extremely painful condition with a few cases reported in the literature,...
Related ArticlesPrimary intradural cervical spine melanocytoma: A rare tumor and review of literature. Neurol India. 2017 May-Jun;65(3):653-657 Authors: Gupta PK, Misra S, Verma R, Soni N, Lamin JC, Mishra RK, Behari S, Kumar S PMID: 28488646 [PubMed - indexed for MEDLINE]
Related ArticlesPost-discectomy annular pseudocyst: A rare cause of failed back syndrome. Neurol India. 2017 May-Jun;65(3):650-652 Authors: Prasad GL, Menon GR PMID: 28488645 [PubMed - indexed for MEDLINE]
Related ArticlesPrepubertal vulvar fibroma, a rare entity little known to dermatologists: report of two cases. J Eur Acad Dermatol Venereol. 2017 Oct;31(10):e448-e449 Authors: Nguyen S, Fraitag S, Cardot-Leccia N, Lagrange S, Trastour C, Passeron T, Croce S, Coindre JM, Lacour JP, Montaudié H PMID: 28419575 [PubMed - indexed for MEDLINE]
Related ArticlesRecent advances in the management of renal cell carcinoma-a radiation oncology perspective. Niger J Clin Pract. 2017 04;20(4):399-408 Authors: Abdus-Salam AA, Olabumuyi AA, Jimoh MA Abstract Renal cell carcinoma (RCC) is a rare cancer in developing countries like Nigeria. However, with an increasing understanding of its epidemiology, the increasing availability of trained personnel, improvement in diagnostic facilities, and greater awareness...
Related ArticlesA Giant Deep-seated Lipoma in a Child's Forearm. J Hand Surg Asian Pac Vol. 2017 Mar;22(1):97-99 Authors: Slavchev SA, Georgiev GP Abstract Deep-seated giant lipomas are rare relative to the overall incidence of the tumor and their occurrence grows more frequent with age. A case of an unusual deep-seated giant lipoma in the forearm of a four-year-old child is reported.PMID: 28205466 [PubMed - indexed for MEDLINE]
Related ArticlesNon-epithelial tumors of the larynx: case series of 12 years. Eur Arch Otorhinolaryngol. 2019 Jun 29;: Authors: Saraydaroglu O, Narter S, Ozsen M, Coskun H Abstract PURPOSE: Laryngeal neoplasms are almost always epithelial in origin and squamous cell carcinoma is the most common tumor of the larynx. Non-epithelial tumors make a small subset of laryngeal neoplasms. We present the experience of a single institution to define clinical presentations...
Related ArticlesThoracic sarcoma case series in Hospital Kuala Lumpur, Malaysia. Med J Malaysia. 2019 Jun;74(3):237-239 Authors: Yurkdes AS, Narasimman S Abstract Thoracic sarcomas (TS) are rare neoplasms that may present with non-specific pulmonary symptoms. Chest radiographs and computed tomography of the thorax are the investigations of choice, while pre-operative minimally invasive biopsies may not be entirely helpful with the diagnosis. The commonly...
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