Πέμπτη 5 Σεπτεμβρίου 2019


A rare case of renal tumor in children: clear cell sarcoma.
Related ArticlesA rare case of renal tumor in children: clear cell sarcoma. G Chir. 2019 May-Jun;40(3):217-224 Authors: Brillantino C, Rossi E, Minelli R, Irace D, Castelli L, Zeccolini R, Bignardi E, Tufano A Abstract Clear cell sarcoma of the kidney is an uncommon renal neopla sm of childhood. It represents about 4% of childhood malignant neoplasms and is generally more common in children under 5 years of age. In the present article, we describe the...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
Unique Aberrations in Intimal Sarcoma Identified by Next-Generation Sequencing as Potential Therapy Targets.
Related ArticlesUnique Aberrations in Intimal Sarcoma Identified by Next-Generation Sequencing as Potential Therapy Targets. Cancers (Basel). 2019 Aug 31;11(9): Authors: Roszik J, Khan A, Conley AP, Livingston JA, Groisberg R, Ravi V, Carmagnani Pestana R, Sen S, Subbiah V Abstract Intimal sarcomas are rare and histologically heterogeneous tumors, commonly arising from the pulmonary arteries. They have remained challenging to treat. Few studies in the...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
A rare case of Meigs syndrome in pregnancy.
Related ArticlesA rare case of Meigs syndrome in pregnancy. Pan Afr Med J. 2019;33:36 Authors: Ziruma A, Hukuimwe M, Nyakura M, Majangara R, Venge M Abstract We present a case of Meigs syndrome in a 19 year old woman. We suspected metastatic ovarian cancer after she had presented in her first pregnancy at 12 weeks gestation. Ultrasound scan had confirmed a complex solid mass in the left adnexa, measuring 7cm x 8cm, a viable 12 weeks pregnancy and gross...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
A drug safety evaluation of mogamulizumab for the treatment of cutaneous T-Cell lymphoma.
Related ArticlesA drug safety evaluation of mogamulizumab for the treatment of cutaneous T-Cell lymphoma. Expert Opin Drug Saf. 2019 Sep;18(9):769-776 Authors: Afifi S, Mohamed S, Zhao J, Foss F Abstract Introduction: Cutaneous T-cell lymphomas (CTCL) are rare non-Hodgkin lymphomas of skin-homing T-cells that initially or mainly manifest cutaneously. Treatment of CTCL is challenging given the disease states' varying presentation and prognosis. Systemic...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
Solitary orbital myofibroma in a child: A rare case report with literature review.
Related ArticlesSolitary orbital myofibroma in a child: A rare case report with literature review. Indian J Ophthalmol. 2019 07;67(7):1240-1245 Authors: Madhuri BK, Tripathy D, Mittal R Abstract Myofibroma is a rare benign mesenchymal tumor of uncertain histogenesis. A six-year-old boy presented with a unilateral lower eyelid mass of six weeks' duration. MRI revealed a circumscribed mass in the inferolateral orbit with bony erosion. A systemic examination...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
Primary lacrimal gland teratoma in an adult: A clinicopathologic and radiological correlation.
Related ArticlesPrimary lacrimal gland teratoma in an adult: A clinicopathologic and radiological correlation. Indian J Ophthalmol. 2019 07;67(7):1238-1240 Authors: Rao R, Honavar SG, Mulay K Abstract A 20-year-old male presented with a gradually growing mass in the left lateral brow region for 2 years. On imaging, the mass appeared to arise from the lacrimal gland, was cystic, without any bony abnormality. With a diagnosis of dermoid cyst, an excision...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
Retinal vascular abnormalities in Sturge-Weber syndrome.
Related ArticlesRetinal vascular abnormalities in Sturge-Weber syndrome. Indian J Ophthalmol. 2019 07;67(7):1223-1226 Authors: Ratra D, Yadav H, Dalan D, Sodhi PKS, Ratra V Abstract Sturge-Weber syndrome (SWS) includes facial, leptomeningeal and choroidal hemangioma. The retinal vasculature is essentially normal. Rare cases of retinal vascular tortuosity and arterio-venous malformations have been reported. We report two cases with rare concomitant...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
Severe hyperlipidemia in a case of acute lymphoblastic leukemia.
Related ArticlesSevere hyperlipidemia in a case of acute lymphoblastic leukemia. Indian J Cancer. 2019 Apr-Jun;56(2):180-181 Authors: Sonowal R, Gupta V Abstract Severe hyperlipidemia (>1000 mg/dL) at initial presentation of acute lymphoblastic leukemia (ALL) is rare. Cases of hyperlipidemia during therapy for childhood ALL where they were secondary to L-asparaginase or steroids have been described. This is a case report of a one-and-half-year-old...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
Concomitant RAS and BRAF mutation in colorectal cancer - A report of 7 cases.
Related ArticlesConcomitant RAS and BRAF mutation in colorectal cancer - A report of 7 cases. Indian J Cancer. 2019 Apr-Jun;56(2):176-179 Authors: Ates O, Yalcin S Abstract Rat sarcoma viral oncogene homolog (RAS) and B-Raf murine sarcoma viral oncogene homolog B1 (BRAF) are members of the same signaling pathway (RAS-RAF-mitogen-activated protein kinase (MAPK) in colorectal cancer (CRC). It is generally assumed that BRAF mutations are seen only with...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
Survival and treatment outcomes of metaplastic breast carcinoma: Single tertiary care center experience in Pakistan.
Related ArticlesSurvival and treatment outcomes of metaplastic breast carcinoma: Single tertiary care center experience in Pakistan. Indian J Cancer. 2019 Apr-Jun;56(2):124-129 Authors: Samoon Z, Beg M, Idress R, Jabbar AA Abstract BACKGROUND: Metaplastic breast carcinoma (MBC) is a rare disease with incidence of less than 1%. MBC present with a larger tumor size, less number of nodes involved, mostly undifferentiated triple negative tumors. We aimed...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
A Rare Case of an Abdominal Aneurysm in a Patient with Lymphangioleiomyomatosis: A Case Report.
Related ArticlesA Rare Case of an Abdominal Aneurysm in a Patient with Lymphangioleiomyomatosis: A Case Report. Perm J. 2019;23: Authors: Chérrez-Ojeda I, Espinoza-Plaza J, Cottin V, Chérrez S Abstract INTRODUCTION: Lymphangioleiomyomatosis (LAM) is a multisystemic disorder characterized by the proliferation, metastasis, and infiltration of smooth muscle cells in the lung and other tissues. Although LAM is rarely seen in men, it is usually detected...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
Matrical carcinoma with melanocytic hyperplasia mimicking nodular melanoma in an elderly Mexican male.
Related ArticlesMatrical carcinoma with melanocytic hyperplasia mimicking nodular melanoma in an elderly Mexican male. J Cutan Pathol. 2019 Jun;46(6):442-446 Authors: Lehmer L, Carly SK, de Feraudy S Abstract Matrical carcinoma with melanocytic hyperplasia (MCMH), previously referred to as malignant melanocytic matricoma, is a rare variant of the uncommon pilomatrical carcinoma, occurring most often on the head/neck and upper backs of middle-aged men....
!@ Rare Cancers
Thu Sep 05, 2019 15:07
Upregulation of transforming growth factor-beta type I receptor by interferon consensus sequence-binding protein in osteosarcoma cells.
Related ArticlesUpregulation of transforming growth factor-beta type I receptor by interferon consensus sequence-binding protein in osteosarcoma cells. Biochim Biophys Acta Mol Cell Res. 2019 05;1866(5):761-772 Authors: Sung JY, Yoon K, Ye SK, Goh SH, Park SY, Kim JH, Kang HG, Kim YN, Park BK Abstract Transforming growth factor-beta (TGF-β) is a known tumor suppressor, which also exerts a tumor promoting activity at an advanced stage of cancer. Previously,...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
Giant renal angiomyolipoma in a solitary kidney.
Related ArticlesGiant renal angiomyolipoma in a solitary kidney. Can J Urol. 2018 12;25(6):9614-9616 Authors: Sohlberg E, Sun A, Massoudi R, Prado K, Skinner E Abstract While renal angiomyolipomas (AMLs) generally remain small and asymptomatic, larger AMLs are more common in tuberous sclerosis patients. Giant AMLs over 20 cm are a rare entity and little is known about their management. We present a unique case of a 48-year-old woman with tuberous sclerosis...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
Anaplastic oligodendroglioma metastasizing to the bone marrow: a unique case report and literature review.
Related ArticlesAnaplastic oligodendroglioma metastasizing to the bone marrow: a unique case report and literature review. Int J Neurosci. 2019 Jul;129(7):722-728 Authors: Singh VK, Singh S, Bhupalam L Abstract Oligodendrogliomas are a rare type of primary brain tumor. They are genetically defined as diffuse gliomas carrying mutation in isocitrate dehydrogenase type 1 (IDH1) or type 2 (IDH2) and codeletion of chromosomes 1p and 19q. The WHO grading...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
ASO Author Reflections: Use of Retrospective Administrative Datasets in Rare Cancer Subtypes to Determine the Efficacy of Adjuvant Therapy.
Related ArticlesASO Author Reflections: Use of Retrospective Administrative Datasets in Rare Cancer Subtypes to Determine the Efficacy of Adjuvant Therapy. Ann Surg Oncol. 2018 12;25(Suppl 3):798-799 Authors: Nassour I, Yopp AC AbstractPMID: 30421055 [PubMed - indexed for MEDLINE]
!@ Rare Cancers
Thu Sep 05, 2019 15:07
Three cases of antibody-LGI1 limbic encephalitis and review of literature.
Related ArticlesThree cases of antibody-LGI1 limbic encephalitis and review of literature. Int J Neurosci. 2019 Jul;129(7):642-648 Authors: Bing-Lei W, Jia-Hua Z, Yan L, Zan Y, Xin B, Jian-Hua S, Hui-Juan W Abstract PURPOSE: Antibody-LGI1 limbic encephalitis (LGI1-Ab LE) is an anti-neuronal surface antigen-related autoimmune encephalitis. we report three cases of LGI1-Ab LE, describe the characteristics of clinical manifestation, course of evolution,...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
Filter-based isolation, enrichment, and characterization of circulating tumor cells.
Related ArticlesFilter-based isolation, enrichment, and characterization of circulating tumor cells. Biotechnol Bioeng. 2018 10;115(10):2504-2529 Authors: Khetani S, Mohammadi M, Nezhad AS Abstract Isolation of circulating tumor cells (CTCs) from blood has long been a challenge due to the rarity and heterogeneity of these cells. Detection technologies have predominantly focused on different molecular or physical properties of CTCs. Size-based isolation...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
Case Report: Orbital Tumor Revealing Adult T-Cell Leukemia/Lymphoma Associated with Human T-Cell Lymphotropic Virus Type-1.
Related ArticlesCase Report: Orbital Tumor Revealing Adult T-Cell Leukemia/Lymphoma Associated with Human T-Cell Lymphotropic Virus Type-1. Am J Trop Med Hyg. 2018 08;99(2):435-438 Authors: Farès S, Hage R, Pegliasco J, Chraibi S, Merle H Abstract Adult T-cell Leukemia/Lymphoma (ATLL) is a sight- and life-threatening complication of human T-cell lymphotropic virus type 1 (HTLV-1) infection. Ophthalmic manifestations include uveitis, optic nerve oedema,...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
Endoscopic port-access approach for excision of left atrial myxoma.
Related ArticlesEndoscopic port-access approach for excision of left atrial myxoma. Multimed Man Cardiothorac Surg. 2018 05 28;2018: Authors: Olsthoorn J, Heuts S, Maessen J, Sardari Nia P Abstract Primary cardiac tumors are a relatively rare disease entity, with myxomas being the most frequently found benign cardiac tumor. After confirmation of this diagnosis, patients are referred for the surgical excision of the tumor. Intracardiac tumors used to...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
[Vascular adrenal cyst causing difficult to control high blood pressure].
Related Articles[Vascular adrenal cyst causing difficult to control high blood pressure]. Hipertens Riesgo Vasc. 2018 Jan - Mar;35(1):37-40 Authors: García Escudero D, Torres Roca M, Hernández Contreras ME, Sánchez Rodríguez C, Oñate Celdrán J Abstract Hypertension is a prevalent disease in developed countries. Adrenal masses, and especially adrenal cysts, are a rare and usually asymptomatic finding, which can go unnoticed or be detected as incidental...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
Primary pituitary diffuse large B-cell lymphoma with somatotroph hyperplasia and acromegaly: case report.
Related ArticlesPrimary pituitary diffuse large B-cell lymphoma with somatotroph hyperplasia and acromegaly: case report. J Neurosurg. 2017 May;126(5):1725-1730 Authors: Ravindra VM, Raheja A, Corn H, Driscoll M, Welt C, Simmons DL, Couldwell WT Abstract Diffuse large B-cell lymphoma (DLBCL) is the most common type of non-Hodgkin lymphoma and comprises approximately 30% of all lymphomas. Patients typically present with a nonpainful mass in the neck,...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
Gamma Knife radiosurgery for glomus jugulare tumors: a single-center series of 75 cases.
Related ArticlesGamma Knife radiosurgery for glomus jugulare tumors: a single-center series of 75 cases. J Neurosurg. 2017 May;126(5):1488-1497 Authors: Ibrahim R, Ammori MB, Yianni J, Grainger A, Rowe J, Radatz M Abstract OBJECTIVE Glomus jugulare tumors are rare indolent tumors that frequently involve the lower cranial nerves (CNs). Complete resection can be difficult and associated with lower CN injury. Gamma Knife radiosurgery (GKRS) has established...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
Gamma Knife radiosurgery for hemangioma of the cavernous sinus.
Related ArticlesGamma Knife radiosurgery for hemangioma of the cavernous sinus. J Neurosurg. 2017 May;126(5):1498-1505 Authors: Lee CC, Sheehan JP, Kano H, Akpinar B, Martinez-Alvarez R, Martinez-Moreno N, Guo WY, Lunsford LD, Liu KD Abstract OBJECTIVE Cavernous sinus hemangiomas (CSHs) are rare vascular tumors. A direct microsurgical approach usually results in massive hemorrhage and incomplete tumor resection. Although stereotactic radiosurgery (SRS)...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
Posterior interosseous nerve discontinuity due to compression by lipoma: report of 2 cases.
Related ArticlesPosterior interosseous nerve discontinuity due to compression by lipoma: report of 2 cases. J Neurosurg. 2017 May;126(5):1698-1701 Authors: Maldonado AA, Howe BM, Spinner RJ Abstract Paralysis of the posterior interosseous nerve (PIN) secondary to compression is a rare clinical condition. Entrapment neuropathy may occur at fibrous bands at the proximal, middle, or distal edge of the supinator. Tumors are a relatively rare but well-known...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
An IDH1-mutated primary gliosarcoma: case report.
Related ArticlesAn IDH1-mutated primary gliosarcoma: case report. J Neurosurg. 2017 Feb;126(2):476-480 Authors: Hsieh JK, Hong CS, Manjila S, Cohen ML, Lo S, Rogers L, Sloan AE Abstract The authors present the case of a primary gliosarcoma with an isocitrate dehydrogenase-1 (IDH1) mutation. A 75-year-old man presented with a 3-day history of multiple focal seizures and was found on MRI to have a 2.2-cm left parietal enhancing mass lesion. Brain MRI for...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
Correlation of the venous angioarchitecture of multiple cerebral cavernous malformations with familial or sporadic disease: a susceptibility-weighted imaging study with 7-Tesla MRI.
Related ArticlesCorrelation of the venous angioarchitecture of multiple cerebral cavernous malformations with familial or sporadic disease: a susceptibility-weighted imaging study with 7-Tesla MRI. J Neurosurg. 2017 Feb;126(2):570-577 Authors: Dammann P, Wrede K, Zhu Y, Matsushige T, Maderwald S, Umutlu L, Quick HH, Hehr U, Rath M, Ladd ME, Felbor U, Sure U Abstract OBJECTIVE Multiple cerebral cavernous malformations (CCMs) are rare lesions that occur...
!@ Rare Cancers
Thu Sep 05, 2019 15:07
[Arterial hypertension during pregnancy: Always preeclampsia?]
Related Articles[Arterial hypertension during pregnancy: Always preeclampsia?] Hipertens Riesgo Vasc. 2017 Apr - Jun;34(2):93-95 Authors: Torres-Courchoud I, Alastrue-Del Castaño V, Cebollada-Del Hoyo J, Bielsa-Rodrigo MA, Sancho-Serrano MA Abstract Cushing's syndrome is a rare condition during pregnancy, but it is associated with serious maternal and fetal complications. The most common etiology during pregnancy is the presence of an adrenocortical...
!@ Rare Cancers
Thu Sep 05, 2019 15:07

Pedal Artery Revascularisation: ‘Bogey’, ‘Birdie’, or ‘Eagle’ in the Treatment of Chronic Limb Threatening Ischaemia?
Publication date: Available online 4 September 2019Source: European Journal of Vascular and Endovascular SurgeryAuthor(s): Jos C. van den Berg
ScienceDirect Publication: European Journal of Vascular and Endovascular Surgery
Thu Sep 05, 2019 12:53

Δεν υπάρχουν σχόλια:

Δημοσίευση σχολίου

Αρχειοθήκη ιστολογίου