Σφακιανάκης Αλέξανδρος
ΩτοΡινοΛαρυγγολόγος
Αναπαύσεως 5 Άγιος Νικόλαος
Κρήτη 72100
00302841026182
00306932607174
alsfakia@gmail.com

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Τετάρτη 19 Αυγούστου 2020

 

Mammary-type Myofibroblastoma of the Pre-sacral Space: A Rare Neoplasm.
Mammary-type Myofibroblastoma of the Pre-sacral Space: A Rare Neoplasm. S D Med. 2020 Aug;73(8):342-345 Authors: Den Hartog T, Ness C, Strand D, Aasen G Abstract INTRODUCTION: Mammary-type myofibroblastoma is a very rare, benign, mesenchymal neoplasm that is histologically identical to a myofibroblastoma of the breast but located in an extra-mammary location. To our knowledge, there have been about 160 cases of extra-mammary myofibroblastoma...
Rare Cancers
Wed Aug 19, 2020 13:49
Survival implication of lymphadenectomy in patients surgically treated for apparent early-stage uterine serous carcinoma.
Survival implication of lymphadenectomy in patients surgically treated for apparent early-stage uterine serous carcinoma. J Gynecol Oncol. 2020 Sep;31(5):e64 Authors: Casarin J, Bogani G, Piovano E, Falcone F, Ferrari F, Odicino F, Puppo A, Bonfiglio F, Donadello N, Pinelli C, Laganà AS, Ditto A, Malzoni M, Greggi S, Raspagliesi F, Ghezzi F Abstract OBJECTIVE: Uterine serous carcinoma (USC) is a rare highly aggressive disease. In the present...
Rare Cancers
Wed Aug 19, 2020 13:49
Incidence and predictors of peritoneal metastases of gynecological origin: a population-based study in the Netherlands.
Incidence and predictors of peritoneal metastases of gynecological origin: a population-based study in the Netherlands. J Gynecol Oncol. 2020 Sep;31(5):e58 Authors: Burg L, Timmermans M, van der Aa M, Boll D, Rovers K, de Hingh I, van Altena A Abstract OBJECTIVE: Peritoneal metastases (PM) are a challenge in gynecological cancers, but its appearance has never been described in a population-based study. Therefore, we describe the incidence of...
Rare Cancers
Wed Aug 19, 2020 13:49
Supervariants identification for breast cancer.
Supervariants identification for breast cancer. Genet Epidemiol. 2020 Aug 17;: Authors: Hu J, Li T, Wang S, Zhang H Abstract In genome-wide association studies, signals associated with rare variants and interactions between genes are hard to detect even when the sample size is in tens of thousands. To overcome these problems, we examine the concept of supervariant. Like the classic concept of the gene, a supervariant is a combination of alleles...
Rare Cancers
Wed Aug 19, 2020 13:49
Cutaneous Manifestations in Pancreatic Diseases-A Review.
Cutaneous Manifestations in Pancreatic Diseases-A Review. J Clin Med. 2020 Aug 12;9(8): Authors: Miulescu R, Balaban DV, Sandru F, Jinga M Abstract Pancreatic pathology, comprising acute and chronic pancreatitis, autoimmune pancreatitis and pancreatic neoplasms, primarily presents with gastrointestinal symptoms and signs; however, it is well recognized that it can also associate a wide range of extra-digestive features. Among these systemic...
Rare Cancers
Wed Aug 19, 2020 13:49
MiR-155-5p and MiR-203a-3p Are Prognostic Factors in Soft Tissue Sarcoma.
MiR-155-5p and MiR-203a-3p Are Prognostic Factors in Soft Tissue Sarcoma. Cancers (Basel). 2020 Aug 12;12(8): Authors: Greither T, Koser F, Holzhausen HJ, Güttler A, Würl P, Kappler M, Wach S, Taubert H Abstract Soft tissue sarcoma (STS) is a heterogeneous group of rare malignancies with a five-year survival rate of approximately 50%. Reliable molecular markers for risk stratification and subsequent therapy management are still needed. Therefore,...
Rare Cancers
Wed Aug 19, 2020 13:49
Neoadjuvant Systemic Treatment of Primary Angiosarcoma.
Neoadjuvant Systemic Treatment of Primary Angiosarcoma. Cancers (Basel). 2020 Aug 12;12(8): Authors: Heinhuis KM, IJzerman NS, van der Graaf WTA, Kerst JM, Schrage Y, Beijnen JH, Steeghs N, van Houdt WJ Abstract Angiosarcoma is an extremely rare and aggressive malignancy. Standard of care of localized tumors includes surgery ± radiation. Despite this multimodal treatment, >50% of the angiosarcoma patients develop local or distant recurrent...
Rare Cancers
Wed Aug 19, 2020 13:49
Single-port laparoscopic Deloyers procedure for tension-free anastomosis after extended left colectomy or subtotal colectomy: A 6-patient case series.
Related Articles Single-port laparoscopic Deloyers procedure for tension-free anastomosis after extended left colectomy or subtotal colectomy: A 6-patient case series. Medicine (Baltimore). 2020 Jul 31;99(31):e21421 Authors: Choi BJ, Kwon W, Baek SH, Jeong WJ, Lee SC Abstract Right colon-to-rectal anastomosis is performed in relatively rare conditions, including after subtotal colectomy or extended left hemicolectomy. One technique of tension-free...
Rare Cancers
Wed Aug 19, 2020 13:49
Elevated procalcitonin levels in primary hepatic neuroendocrine carcinoma: Case report and literature review.
Related Articles Elevated procalcitonin levels in primary hepatic neuroendocrine carcinoma: Case report and literature review. Medicine (Baltimore). 2020 Jul 31;99(31):e21210 Authors: Han X, Zhong H, Hong D, Li C, Su H, Xu K Abstract RATIONALE: Procalcitonin (PCT) has been identified as a tumor biomarker in medullary thyroid carcinoma. Other neuroendocrine carcinomas with elevated PCT levels are relatively rare, and are mainly reported in...
Rare Cancers
Wed Aug 19, 2020 13:49
Ovarian metastasis in women with cervical carcinoma in stages IA to IIB: A systematic review and meta-analysis.
Related Articles Ovarian metastasis in women with cervical carcinoma in stages IA to IIB: A systematic review and meta-analysis. Medicine (Baltimore). 2020 Jul 31;99(31):e21146 Authors: Fan Y, Wang MY, Mu Y, Mo SP, Zheng A, Li JK Abstract BACKGROUND: Cervical cancer is one of the common malignancies that afflict women worldwide. In rare cases, cervical cancer leads to ovarian metastasis (OM), resulting in poor outcomes. We conducted a systematic...
Rare Cancers
Wed Aug 19, 2020 13:49
A Rare Case of Bicytopenia and Peritoneal Lymphadenopathy.
Related Articles A Rare Case of Bicytopenia and Peritoneal Lymphadenopathy. Isr Med Assoc J. 2020 Jul;7(22):386-388 Authors: Tocut M, Vaknine H, Potachenko P, Elias S, Zandman-Goddard G PMID: 32692503 [PubMed - indexed for MEDLINE]
Rare Cancers
Wed Aug 19, 2020 13:49
Marriage of black phosphorus and Cu2+ as effective photothermal agents for PET-guided combination cancer therapy.
Related Articles Marriage of black phosphorus and Cu2+ as effective photothermal agents for PET-guided combination cancer therapy. Nat Commun. 2020 06 08;11(1):2778 Authors: Hu K, Xie L, Zhang Y, Hanyu M, Yang Z, Nagatsu K, Suzuki H, Ouyang J, Ji X, Wei J, Xu H, Farokhzad OC, Liang SH, Wang L, Tao W, Zhang MR Abstract The use of photothermal agents (PTAs) in cancer photothermal therapy (PTT) has shown promising results in clinical studies....
Rare Cancers
Wed Aug 19, 2020 13:49
Mortality and risk of progression to adult T cell leukemia/lymphoma in HTLV-1-associated myelopathy/tropical spastic paraparesis.
Related Articles Mortality and risk of progression to adult T cell leukemia/lymphoma in HTLV-1-associated myelopathy/tropical spastic paraparesis. Proc Natl Acad Sci U S A. 2020 05 26;117(21):11685-11691 Authors: Nagasaka M, Yamagishi M, Yagishita N, Araya N, Kobayashi S, Makiyama J, Kubokawa M, Yamauchi J, Hasegawa D, Coler-Reilly ALG, Tsutsumi S, Uemura Y, Arai A, Takata A, Inoue E, Hasegawa Y, Watanabe T, Suzuki Y, Uchimaru K, Sato T, Yamano Y ...
Rare Cancers
Wed Aug 19, 2020 13:49
[Radiologic Features of Nuclear Protein of the Testis Midline Carcinoma of the Nasal Cavity and Paranasal Sinuses:Report of One Case].
Related Articles [Radiologic Features of Nuclear Protein of the Testis Midline Carcinoma of the Nasal Cavity and Paranasal Sinuses:Report of One Case]. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2020 Apr 28;42(2):279-282 Authors: He XY, Liu ZH, Zhang Q Abstract Nuclear protein of the testis midline carcinoma (NMC) is a rare malignant tumor that is mostly located in the upper trachea,mediastinal midline,and paravertebral midline,and few literature...
Rare Cancers
Wed Aug 19, 2020 13:49
An infant with intradural extramedullary synovial sarcoma: the youngest case in the literature.
Related Articles An infant with intradural extramedullary synovial sarcoma: the youngest case in the literature. Turk J Pediatr. 2019;61(5):765-770 Authors: Yalçın K, Tüysüz G, Kazan S, Gürer Eİ, Karaali K, Küpesiz A, Güler E Abstract Yalçın K, Tüysüz G, Kazan S, Gürer Eİ, Karaali K, Küpesiz A, Güler E. An infant with intradural extramedullary synovial sarcoma: the youngest case in the literature. Turk J Pediatr 2019; 61: 765-770. Spinal cord...
Rare Cancers
Wed Aug 19, 2020 13:49
Ewing sarcoma in an infant and review of the literature.
Related Articles Ewing sarcoma in an infant and review of the literature. Turk J Pediatr. 2019;61(5):760-764 Authors: Bedük-Esen ÇS, Gültekin M, Aydın GB, Akyüz C, Oğuz KK, Orhan D, Cengiz M, Gürkaynak M, Yıldız F Abstract Bedük Esen ÇS, Gültekin M, Aydın GB, Akyüz C, Karlı Oğuz K, Orhan D, Cengiz M, Gürkaynak M, Yıldız F. Ewing sarcoma in an infant and review of the literature. Turk J Pediatr 2019; 61: 760-764. Ewing sarcoma (ES) is a rare...
Rare Cancers
Wed Aug 19, 2020 13:49
Fetal intrapericardial teratomas.
Related Articles Fetal intrapericardial teratomas. Turk J Pediatr. 2019;61(2):153-158 Authors: Yuan SM, Lin H Abstract Yuan SM, Lin H. Fetal intrapericardial teratomas. Turk J Pediatr 2019; 61: 153-158. Fetal intrapericardial teratomas are rare and benign. However, they can be life-threatening owing to the complicated massive pericardial effusions, tamponade, or cardiorespiratory distress. The purpose of this review is to give an overview on...
Rare Cancers
Wed Aug 19, 2020 13:49
Surgical management of spinal intramedullary tumors: Ten-year experience in a single institution.
Related Articles Surgical management of spinal intramedullary tumors: Ten-year experience in a single institution. J Clin Neurosci. 2020 Mar;73:201-208 Authors: Alizada O, Kemerdere R, Ulu MO, Akgun MY, Isler C, Kizilkilic O, Hanci MM Abstract Despite their rare occurrence, intramedullary spinal cord tumors can cause considerable morbidity and mortality without treatment. Timing of surgery, extent of resection and selection of favorable treatment...
Rare Cancers
Wed Aug 19, 2020 13:49
Postoperative pancreatic fistula after distal pancreatectomy for non-pancreas retroperitoneal tumor resection.
Related Articles Postoperative pancreatic fistula after distal pancreatectomy for non-pancreas retroperitoneal tumor resection. Am J Surg. 2020 07;220(1):140-146 Authors: Keung EZ, Asare EA, Chiang YJ, Prakash LR, Rajkot N, Torres KE, Hunt KK, Feig BW, Cormier JN, Roland CL, Katz MHG, Lee JE, Tzeng CD Abstract INTRODUCTION: Short-term outcomes after distal pancreatectomy (DP) for retroperitoneal (RP) tumors are unknown. We sought to identify...
Rare Cancers
Wed Aug 19, 2020 13:49
Partial Response to Ceritinib in a Patient With Abdominal Inflammatory Myofibroblastic Tumor Carrying a TFG-ROS1 Fusion.
Related Articles Partial Response to Ceritinib in a Patient With Abdominal Inflammatory Myofibroblastic Tumor Carrying a TFG-ROS1 Fusion. J Natl Compr Canc Netw. 2019 12;17(12):1459-1462 Authors: Li Y, Chen X, Qu Y, Fan JM, Li Y, Peng H, Zheng Y, Zhang Y, Zhang HB Abstract Inflammatory myofibroblastic tumor (IMT), a rare sarcoma, is primarily treated via resection of the mass. However, there is no standard treatment for recurrence or unresectable...
Rare Cancers
Wed Aug 19, 2020 13:49
Some mutations in the xeroderma pigmentosum D gene may lead to moderate but significant radiosensitivity associated with a delayed radiation-induced ATM nuclear localization.
Related Articles Some mutations in the xeroderma pigmentosum D gene may lead to moderate but significant radiosensitivity associated with a delayed radiation-induced ATM nuclear localization. Int J Radiat Biol. 2020 03;96(3):394-410 Authors: Ferlazzo M, Berthel E, Granzotto A, Devic C, Sonzogni L, Bachelet JT, Pereira S, Bourguignon M, Sarasin A, Mezzina M, Foray N Abstract Purpose: Xeroderma Pigmentosum (XP) is a rare, recessive genetic disease...
Rare Cancers
Wed Aug 19, 2020 13:49
Rare Case of Thoracic Desmoplastic Small Round Cell Tumor in a Three-Year-Old Boy.
Related Articles Rare Case of Thoracic Desmoplastic Small Round Cell Tumor in a Three-Year-Old Boy. J Oncol Pract. 2019 11;15(11):617-620 Authors: Suhag S, Byrd RH, Jaiswal K PMID: 31618088 [PubMed - indexed for MEDLINE]
Rare Cancers
Wed Aug 19, 2020 13:49
Integrated clinical, histopathological, and molecular data analysis of 190 central nervous system germ cell tumors from the iGCT Consortium.
Related Articles Integrated clinical, histopathological, and molecular data analysis of 190 central nervous system germ cell tumors from the iGCT Consortium. Neuro Oncol. 2019 12 17;21(12):1565-1577 Authors: Takami H, Fukuoka K, Fukushima S, Nakamura T, Mukasa A, Saito N, Yanagisawa T, Nakamura H, Sugiyama K, Kanamori M, Tominaga T, Maehara T, Nakada M, Kanemura Y, Asai A, Takeshima H, Hirose Y, Iuchi T, Nagane M, Yoshimoto K, Matsumura A, Kurozumi K, Nakase...
Rare Cancers
Wed Aug 19, 2020 13:49
HPV RNA in-situ hybridization as a diagnostic aid in papillary laryngeal lesions.
Related Articles HPV RNA in-situ hybridization as a diagnostic aid in papillary laryngeal lesions. Laryngoscope. 2020 04;130(4):955-960 Authors: Garcia JA, Best SR, Rooper LM Abstract OBJECTIVES: In the larynx, differentiating squamous papillomas from de-novo papillary squamous dysplasias or squamous cell carcinomas (SCC) has significant consequences for management. Overlapping clinical presentations and cytologic changes across the spectrum...
Rare Cancers
Wed Aug 19, 2020 13:49
StatPearls
StatPearls Book. 2020 01 Authors: Abstract Mediastinal carcinoid tumors are represented by thymic carcinoid neoplasms. Primary carcinoid tumors of the thymus were first described in 1972.[1] The term carcinoid is an old term that refers to a carcinoma-like appearance of the tumors and is often used interchangeably with neuroendocrine tumors (NETs). Thymic carcinoid tumors are rare neoplasms arising from the thymus deriving from the foregut, being the least common...
Rare Cancers
Wed Aug 19, 2020 13:49
StatPearls
StatPearls Book. 2020 01 Authors: Abstract Oral hemangiomas (OHs) are benign tumors that develop due to endothelial cell proliferation and occur in and around the oral cavity. While 60 to 70 percent of hemangiomas occur in the head and neck region, OHs are relatively rare and most frequently involve the lips, tongue, buccal mucosa, and palate. OHs have also been noted in the mandible and maxilla (central hemangiomas) and within the masseter and other muscles...
Rare Cancers
Wed Aug 19, 2020 13:49
StatPearls
StatPearls Book. 2020 01 Authors: Abstract The parotid gland is salivary gland others include submandibular and sublingual glands. It is enclosed within a fascial capsule and comprises a superficial lobe and a deep lobe separated by the facial nerve. It is an exocrine gland that secretes saliva into the oral cavity after parasympathetic stimulation. The Stensen canal is the primary excretory duct for the parotid gland, passing through the masseter muscles, penetrating...
Rare Cancers
Wed Aug 19, 2020 13:49

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