Related ArticlesType A insulin resistance syndrome misdiagnosed as polycystic ovary syndrome: a case report. J Med Case Rep. 2019 Nov 27;13(1):347 Authors: Lin L, Chen C, Fang T, Chen D, Chen K, Quan H Abstract BACKGROUND: Type A insulin resistance syndrome, one type of the hereditary insulin resistance syndromes, is a rare disorder. Patients with type A insulin resistance syndrome are nonobese and demonstrate severe hyperinsulinemia, hyperandrogenism,...
Related ArticlesSuccessful Treatment of Hypokalemic Rhabdomyolysis Caused by a Pancreatic VIPoma: A Case Report. Am J Case Rep. 2019 Nov 22;20:1723-1727 Authors: Ramirez S, Lytle M, Togores E, Parellada J, Carlan SJ, Madruga M, Murillo-Alvarez RM Abstract BACKGROUND VIPomas are rare neuroendocrine tumors typically located in the pancreas. The majority of cases autonomously secret vasoactive intestinal polypeptide (VIP), which can result in profuse,...
Related ArticlesHuman Leukocyte Antigen (HLA) Subtype-Dependent Development of Myasthenia Gravis, Type-1 Diabetes Mellitus, and Hashimoto Disease: A Case Report of Autoimmune Polyendocrine Syndrome Type 3. Am J Case Rep. 2019 Nov 20;20:1709-1714 Authors: Gobaru M, Ashida K, Yoshinobu S, Nagayama A, Kabashima M, Iwata S, Hasuzawa N, Tsuruta M, Wada N, Nakayama H, Motomura S, Tajiri Y, Nomura M Abstract BACKGROUND Patients with type 1 diabetes mellitus,...
Related ArticlesSpinal Intradural Extramedullary Ependymoma with Intracranial Metastasis and Leptomeningeal Spread: A Case Report and Comprehensive Review of Literature. Neurol India. 2019 Sep-Oct;67(5):1352-1357 Authors: Garg K, Sharma R, Dash C, Agrawal D, Sharma BS Abstract Dorsolumbar intradural extramedullary ependymoma is a rare entity. Spinal metastases in patients with intracranial ependymoma are well described, but it is extremely rare for...
Related ArticlesIntracranial Myoepithelioma: A Case Report and Review of Literature. Neurol India. 2019 Sep-Oct;67(5):1347-1351 Authors: Gowripriya G, Sridhar K, Vij M Abstract Intracranial myoepithelial tumors are extremely rare with <10 cases reported outside the sellar region. The authors describe a case of a 43-year-old male patient who presented with headache, numbness in the face, and a dumbbell-shaped lesion in the Meckel's cave clinically...
Related ArticlesTumor-induced Osteomalacia due to a Phosphaturic Mesenchymal Tumor in the Cervical Spine: A Case Report and Literature Review. Neurol India. 2019 Sep-Oct;67(5):1334-1340 Authors: Agarwal N, Kale SS, Kumari K Abstract Tumor-induced osteomalacia (TIO) is a rare paraneoplastic syndrome of certain mesenchymal tumors which secrete fibroblast growth factor-23 (FGF-23) responsible for causing features of hypophosphatemia and osteomalacia in...
Related ArticlesA Pericallosal Lipoma Case with Abnormal Vasculature Mimicking Arteriovenous Malformation. Neurol India. 2019 Sep-Oct;67(5):1331-1333 Authors: Erbay MF, Tecellioglu M Abstract Pericallosal lipomas (PCLs) are rare tumors of the central nervous system. They may be associated with some parenchymal and vascular anomalies of brain. Magnetic resonance imaging is the modality of choice to assess the extent of the PCLs and possible concomitant...
Related ArticlesPort-Site Implantation Diagnosed by Iodine-131 Post-Ablation Single-Photon Emission Tomography-Computed Tomography After Robotic Thyroidectomy: A Case Report. Am J Case Rep. 2019 Nov 18;20:1695-1698 Authors: Kim MR, Jo S, Shim HK Abstract BACKGROUND Robotic thyroidectomy using remote access approaches is currently regarded as the optimal surgical protocol for highly selected patients. This approach has excellent cosmetic outcomes compared...
Related ArticlesClinicopathologic features of Buschke-Löwenstein tumor: a multi-institutional analysis of 38 cases. Virchows Arch. 2020 Apr;476(4):543-550 Authors: Zhang D, Gonzalez RS, Feely M, Umrau K, Lee H, Allende DS, Karamchandani DM, Zaleski M, Lin J, Westerhoff M, Zhang X, Alpert L, Liao X, Lai J, Liu X Abstract Buschke-Löwenstein tumor (BLT) is a rare sexually transmitted disease, mostly described in clinical literature as case reports or small...
Related ArticlesLong-term multidisciplinary integrative therapy management resulted in favorable outcomes for ovarian cancer during pregnancy: a case report and literature review. J Ovarian Res. 2019 Nov 11;12(1):108 Authors: Xu T, Wang L, Jia Y, Jia Z, Li Z, Cui S, Cui M Abstract BACKGROUND: Ovarian cancer during pregnancy is relatively rare and treatment strategies are inexperienced in surgery and chemotherapy. Multidisciplinary management of advanced...
Related ArticlesGiant cell tumor of the thoracic spine in a 30-year-old woman. JAAPA. 2019 Nov;32(11):1-3 Authors: Shivers J, Hu X, Lieberman IH Abstract Giant cell tumor (GCT) of the spine is a rare, benign tumor. Patients typically present with pain and also may experience neurologic deficits from spinal cord and/or nerve root compression. This article describes a patient who presented with acute mid-back pain, was diagnosed with spinal GCT through...
Related ArticlesSolitary fibrous tumor: a case series identifying pathological adverse factors-implications for risk stratification and classification. Virchows Arch. 2020 Apr;476(4):597-607 Authors: Machado I, Morales GN, Cruz J, Lavernia J, Giner F, Navarro S, Ferrandez A, Llombart-Bosch A Abstract Solitary fibrous tumors (SFTs) are a rare type of mesenchymal lesion in which specific clinicopathologic factors have been related to patient outcome....
Related ArticlesAcquired haemophilia A in a patient with breast cancer and lung carcinoma: a case report and literature review. Neth J Med. 2019 05;77(4):153-155 Authors: Biesheuvel V, Hiddema SM, Levenga H, Eikenboom J, van der Deure WM Abstract Acquired haemophilia A is a rare disorder caused by spontaneous formation of auto-antibodies (inhibitors) against coagulation factor VIII. This can lead tolife-threatening haemorrhages. Six to twenty-two percent...
Related ArticlesAnticancer Effects of Constituents of Herbs Targeting Osteosarcoma. Chin J Integr Med. 2019 Dec;25(12):948-955 Authors: Su QH, Xu XQ, Wang JF, Luan JW, Ren X, Huang HY, Bian SS Abstract Osteosarcoma is a rare primary malignancy of bone that is prone to early metastasis. Resection surgery and chemotherapeutic regimens are current standard treatments for osteosarcoma. However, the long-term survival rate of patients with osteosarcoma is...
Related ArticlesAtypical fibroxanthoma arising in a tracheostomy scar: A rare cicatricial neoplasm. Australas J Dermatol. 2019 Nov;60(4):327-328 Authors: Byth LA, Strutton GM PMID: 31049929 [PubMed - indexed for MEDLINE]
Related ArticlesProgressive late-onset porokeratotic eccrine ostial and dermal duct naevus. Australas J Dermatol. 2019 Nov;60(4):e333-e334 Authors: Vahabi-Amlashi S, Tayyebi Meibodi N, Feli S, Taghavi F PMID: 30989652 [PubMed - indexed for MEDLINE]
Related ArticlesTotally endoscopic robotic-assisted excision of right ventricular papillary fibroelastoma. J Robot Surg. 2019 Dec;13(6):779-782 Authors: Nisivaco S, Henry M, Ward RP, Balkhy HH Abstract Although they comprise a small number of primary tumors of the heart, papillary fibroelastomas (PFEs) are the second most common type of benign cardiac tumor. PFEs of the right heart are uncommon, and those arising from the right-ventricular (RV) wall...
Related ArticlesMalignant ovarian germ cell tumours in the post-menopausal population. Aust N Z J Obstet Gynaecol. 2019 04;59(2):285-287 Authors: Robertson JA, Sanday K, Nicklin J Abstract BACKGROUND: Malignant ovarian germ cell tumours (MOGCT) are uncommon in the general population and very rare in post-menopausal women. AIMS: To evaluate the demographics, treatment and survival of post-menopausal women with MOGCT treated at the Queensland...
Related ArticlesRetroperitoneal fibrosis associated with immunoglobulin IgG4-related disease in the differential diagnosis in retroperitoneal tumors. Case report. Reumatol Clin. 2019 Sep - Oct;15(5):e27-e29 Authors: Ruiz Mar G, Cárdenas Serrano ÓE, Roldan García J, Cañavera-Constantino A, Menéndez Trejo VM, Chapa Azuela Ó Abstract The patient was a 55-year-old woman with a 4-month history of pain in left flank that irradiated to the lumbar region. Computed...
Related ArticlesNon-Hodgkin's lymphoma and atypical neck pain: A case report. Reumatol Clin. 2019 Sep - Oct;15(5):e44-e46 Authors: Rojas N, Fernandes C, Conde M, Montala N, Fornos X, Rosselló L, Pallisó F Abstract Neck pain is a common reason for seeking medical attention. It affects at least 15% of the labor force and up to 40% of individuals whose occupation is hazardous. On the other hand, primary bone lymphoma is a very rare disease (less than 1%...
Leiomyosarcoma of renal vein: A case report. Urol Case Rep. 2020 Jul;31:101186 Authors: Manoj Kumar G, Nirmal KP Abstract Leiomyosarcoma of the renal vein is a rare tumor of complex diagnosis. We present a case of renal vein leiomyosarcoma in a patient presented with left flank pain. The patient underwent radical nephrectomy with tumour excision.PMID: 32322515 [PubMed]
SEER and Gene Expression Data Analysis Deciphers Racial Disparity Patterns in Prostate Cancer Mortality and the Public Health Implication. Sci Rep. 2020 Apr 22;10(1):6820 Authors: Zhang W, Dong Y, Sartor O, Flemington EK, Zhang K Abstract A major racial disparity in prostate cancer (PCa) is that African American (AA) patients have a higher mortality rate than European American (EA) patients. We filtered the SEER 2009-2011 records and divided them into...
Related ArticlesDe-differentiation of papillary thyroid carcinoma into squamous cell carcinoma in an elderly patient: A case report. Medicine (Baltimore). 2020 Apr;99(16):e19892 Authors: Thewjitcharoen Y, Krittiyawong S, Butadej S, Nakasatien S, Polchart S, Junyangdikul P, Kanchanapituk A, Himathongkam T Abstract RATIONALE: The unpredictability of thyroid cancer can be striking, as the disease may rapidly progress to death in some individuals. Herein,...
Related ArticlesSurgical treatment of asymptomatic epithelioid hemangioendothelioma originating from the superior vena cava: A case report. Medicine (Baltimore). 2020 Apr;99(16):e19859 Authors: Lee SS, Lee JH Abstract RATIONALE: Epithelioid hemangioendothelioma is a rare endothelial tumor with a low-grade malignancy. This tumor can be treated with complete resection. PATIENT CONCERNS: A 20-year-old Korean man visited our hospital due to an...
Related ArticlesRecurrence of pigmented villonodular synovitis of the knee: A case report with review of literature on the risk factors causing recurrence. Medicine (Baltimore). 2020 Apr;99(16):e19856 Authors: Fang Y, Zhang Q Abstract RATIONALE: Pigmented villonodular synovitis is a rare disease which may involve any joints. It has localized and diffuse forms, and the latter is more aggressive with a higher recurrence rate. Different treatments are...
Related Articles[Clinicopathologic features of testicular seminoma with syncytiotrophoblastic cells: Analysis of 3 cases and review of the literature]. Zhonghua Nan Ke Xue. 2019 Jul;25(7):642-646 Authors: Liang Y, Tu P, Wang X, Yi XM, Zhou XD, Shi QL Abstract Objective: To investigate the clinical and histopathologic features of testicular seminoma with syncytoplasmic trophoblastic components. METHODS: Using light microscopic staining, we analyzed...
Related Articles[Analysis of misdiagnosis causes of suprasellar arachnoid cysts]. Zhonghua Yi Xue Za Zhi. 2020 Mar 03;100(8):610-613 Authors: Qu Z, Zong XY, Li JH, Qian T, Ni HT Abstract Objective: To investigate the causes of misdiagnosis of suprasellar arachnoid cysts, analyze its characteristics and put forward the diagnostic basis and differential points. Methods: The clinical data fo 97 cases of suprasellar arachnoid cysts diagnosed and treated...
Related Articles11-year experience with Chest Wall resection and reconstruction for primary Chest Wall sarcomas. J Cardiothorac Surg. 2020 Jan 28;15(1):29 Authors: Wald O, Islam I, Amit K, Ehud R, Eldad E, Omer O, Aviad Z, Moshe SO, Uzi I Abstract BACKGROUND & OBJECTIVES: Primary chest wall sarcomas are rare and therapeutically challenging tumors. Herein we report the outcomes of a surgery-based multimodality therapy for these pathologies over...
Related ArticlesHow can we manage patients over forty with endometriosis? Minerva Med. 2020 Feb;111(1):62-67 Authors: Oral E, Inceboz U Abstract Peri/postmenopausal endometriosis is not as rare as once we thought. Accumulated data revealed that around 1/3-1/4 of women with surgically-diagnosed endometriosis after the age of 40. The uneasiness of the issue of malignant transformation or malignancy in such women created a challenge for us. Here the management...
Related ArticlesTeenager with Cystic Swelling in the Floor of the Mouth. Indian Pediatr. 2019 10 15;56(10):891 Authors: Sharawat IK, Kumar A, Dawman L PMID: 31724554 [PubMed - indexed for MEDLINE]
Related ArticlesCan Less Intensive Chemotherapy and an Autotransplant Cure Adult T-Cell Acute Lymphoblastic Leukemia? Acta Haematol. 2020;143(2):131-139 Authors: Parovichnikova E, Troitskaya V, Sokolov A, Gavrilina O, Akhmerzaeva Z, Kuzmina L, Kliasova G, Chabaeva J, Kulikov S, Bondarenko S, Baranova O, Samoilova O, Kaplanov K, Minaeva N, Savchenko V, Russian Acute Lymphoblastic Leukemia Group Abstract T-cell acute lymphoblastic leukemia (T-ALL) is...
Related ArticlesHematologic malignancies of the larynx: A single institution review. Am J Otolaryngol. 2019 Nov - Dec;40(6):102285 Authors: Dewan K, Campbell R, Damrose EJ Abstract BACKGROUND: Primary hematologic malignancies of the larynx are rare diagnoses, accounting for less than 1% of all laryngeal tumors. They most commonly present as submucosal masses of the supraglottis, with symptoms including hoarseness, dysphagia, dyspnea and rarely cervical...
Related ArticlesLong-term Outcome After Resection of Isolated Thoracic Lymph Node Metastases of Renal Cell Cancer. Ann Thorac Surg. 2020 01;109(1):262-269 Authors: Sponholz S, Schirren M, Oguzhan S, Mese M, Schirren J Abstract BACKGROUND: Isolated thoracic lymph node metastases (ITLNMs) without any lung metastases of renal cell cancer are rare. Other than a few case reports and one study, there is no further literature on ITLNMs. For this reason, the...
Related ArticlesCarcinoma ex pleomorphic adenoma: A review of incidence, demographics, risk factors, and survival. Am J Otolaryngol. 2019 Nov - Dec;40(6):102279 Authors: Gupta A, Koochakzadeh S, Neskey DM, Nguyen SA, Lentsch EJ Abstract PURPOSE: Identify variables that are independent predictors of survival in carcinoma ex pleomorphic adenoma (CXPA) of the major salivary glands using a population-based database and evaluate the incidence and management...
Related ArticlesCommentary: Solitary Fibrous Tumor of the Esophagus-Rare but With Typical Characteristics. Semin Thorac Cardiovasc Surg. 2020;32(1):179-180 Authors: Yeung J, de Perrot M PMID: 31442492 [PubMed - indexed for MEDLINE]
Related ArticlesSquamous Cell Carcinoma in Lichen Planus of the Esophagus. Ann Thorac Surg. 2020 02;109(2):e83-e85 Authors: Thomas M, Makey IA, Francis DL, Wolfsen HC, Bowers SP Abstract Cancer arising in lichen planus of the esophagus (LPE) is extremely rare. We report 2 elderly female patients with LPE who developed squamous cell carcinoma. Both underwent laparoscopic ischemic gastric preconditioning followed 2 weeks later by 3-field esophagectomy....
Related ArticlesNecrotizing Hemorrhagic Gastritis following Acute Myeloid Leukemia Induction with Midostaurin: An Unexpected Complication. Acta Haematol. 2020;143(1):65-68 Authors: Shimony S, Reiss Mintz H, Shvartser Beryozkin Y, Shoham A, Raanani P, Wolach O Abstract Midostaurin is a tyrosine multikinase inhibitor approved for the treatment of patients with newly diagnosed acute myeloid leukemia (AML) with mutated Fms-like tyrosine kinase-3. We describe...
Related ArticlesA Rare Pulmonary Artery Sarcoma Masquerading as Pulmonary Embolus. Ann Thorac Surg. 2020 02;109(2):e103-e105 Authors: Skiba R, Stamp N, Kehoe M, Merry C Abstract We present the case of a 46-year-old woman with a presumed diagnosis of multiple unprovoked pulmonary emboli. Her cardiorespiratory function continued to deteriorate despite optimal medical therapy. At surgical thrombectomy she was identified to have an intimal soft tissue lesion...
Related ArticlesComplex Lobectomy in a Patient With Lung Cancer and Pulmonary Artery Sling. Ann Thorac Surg. 2020 01;109(1):e55-e57 Authors: Mammana M, Zuin A, Serra E, Bellini A, Rea F Abstract Pulmonary artery sling is a rare congenital anomaly of the origin and course of the left pulmonary artery. Patients with this condition typically present with respiratory failure in young infancy, and asymptomatic cases are uncommon. We describe the case of...
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