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Artykuły w czasopismach na temat „Rare sites”

Autor: Grafiati

Data publikacji: 7 czerwca 2025

Data aktualizacji: 2 sierpnia 2025

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1

Sutherland, G. R. "Rare fragile sites." Cytogenetic and Genome Research 100, no. 1-4 (2003): 77–84. http://dx.doi.org/10.1159/000072840.

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2

Ballard, Billy. "Neuroendocrine Carcinomas of Rare Sites." Journal of the National Medical Association 112, no. 5 (2020): S40—S41. http://dx.doi.org/10.1016/j.jnma.2020.09.115.

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3

Medlock, K., and M. Thomas. "Not so rare Internet sites." Anaesthesia 57, no. 5 (2002): 501–21. http://dx.doi.org/10.1046/j.1365-2044.2002.262632.x.

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4

Ambhika, Nalla, Ranganath Ratnagiri, Megha Uppin, and Sujata Patnaik. "A Case Report of A Rare Tumor In Rare Site." International Journal of Orthopaedics Research 7, no. 3 (2024): 01–05. https://doi.org/10.33140/ijor.07.03.02.

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Synovial sarcoma is a rare soft tissue tumour occurring in young ages. Most common site is extremities close to joints. Thoracic wall, chest and trunk are rare sites. Presence of calcifications, hemorrhage, solid, cystic / necrotic component and triple sign in MRI are characteristic. This is a case report of synovial sarcoma in the right supraclavicular fossa extending along chest wall. Its radiological features are described.

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5

Tutun, Sule, Levent Ozgonenel, Esra Cetin, and Ebru Aytekin. "Two rare involvement sites: synovial chondromatosis." Rheumatology International 31, no. 5 (2009): 687–89. http://dx.doi.org/10.1007/s00296-009-1224-9.

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6

Romain, D. R., L. M. Columbano-Green, R. H. Smythe, R. G. Parfitt, O. B. Gebbie, and C. J. Chapman. "Studies on three rare fragile sites." Human Genetics 73, no. 2 (1986): 164–70. http://dx.doi.org/10.1007/bf00291608.

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7

Nemri, Sabah Nayef, Bouvier Francis Valere D’sa, Sohaila Fatima, Nazima Haider, and Nouha Mahmood Alwani. "Extraskeletal Ewing sarcoma at rare sites with review of literature." Annals of Pathology and Laboratory Medicine 4, no. 1 (2017): C9—C13. http://dx.doi.org/10.21276/apalm.2017.1110.

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8

Ahmed, Imtiaz, Divya Shelly, K. V. VinuBalraam, Kriti Agarwal, and Reena Bharadwaj. "Synovial Sarcoma: a Clinicopathological Study with Emphasis on Rare Sites." Annals of Pathology and Laboratory Medicine 5, no. 11 (2018): A848–854. http://dx.doi.org/10.21276/apalm.2086.

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9

Singh, Guddi Rani. "Primary Ewing Sarcoma at Rare Sites – A Study of Few Cases." Journal of Medical Science And clinical Research 05, no. 05 (2017): 21876–80. http://dx.doi.org/10.18535/jmscr/v5i5.105.

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10

Koo, Hee Youn, Myung Jun Lee, Chang Joon Lee, and Jeong Hyun Yoo. "Neurilemmoma at Rare Sites: Two Cases Report." Journal of the Korean Radiological Society 45, no. 6 (2001): 571. http://dx.doi.org/10.3348/jkrs.2001.45.6.571.

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11

Ogose, Akira, Teiichi Motoyama, Tetsuo Hotta, et al. "Clear cell chondrosarcomas arising from rare sites." Pathology International 45, no. 9 (1995): 684–90. http://dx.doi.org/10.1111/j.1440-1827.1995.tb03522.x.

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12

ROBINSON, B. W., and C. S. BENJAMIN. "Extranodal Non-Hodgkins Lymphoma in Rare Sites." Australasian Radiology 31, no. 4 (1987): 418–20. http://dx.doi.org/10.1111/j.1440-1673.1987.tb01864.x.

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13

Carey, Michael Clay. "Facebook Interactivity Rare on Community News Sites." Newspaper Research Journal 35, no. 2 (2014): 119–33. http://dx.doi.org/10.1177/073953291403500209.

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14

Lin, T. K., L. Lichti, C. Boekema, and A. B. Denison. "Muon bonding sites in rare earth orthoferrites." Hyperfine Interactions 31, no. 1-4 (1986): 475–80. http://dx.doi.org/10.1007/bf02401599.

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15

Tufano, Antonella, and Pietro Amedeo Modesti. "The “very rare” unusual sites venous thromboses." Internal and Emergency Medicine 12, no. 6 (2017): 745–47. http://dx.doi.org/10.1007/s11739-017-1701-1.

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16

Sandeep, Ramkrishna Hambarde. "Management and Outcome of Mature Teratomas at Rare Sites: Our Experience." International Journal of Pharmaceutical and Clinical Research 16, no. 12 (2024): 841–47. https://doi.org/10.5281/zenodo.14592201.

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Mature teratomas, although commonly documented in pediatric and young adult populations, can manifest in various rare anatomical locations, posing significant clinical challenges. Understanding the spectrum of their presentations and outcomes is essential for effective diagnosis and management. The purpose of this study was to explore the occurrence, presentation and treatment outcomes of mature teratomas located at unusual sites, contributing to the limited body of knowledge on these rare cases. This was a retrospective analysis conducted at a tertiary care center in Central India, reviewing

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17

Di Micco, Rosa, Letizia Santurro, Maria Luisa Gasparri, et al. "Rare sites of breast cancer metastasis: a review." Translational Cancer Research 8, S5 (2019): S518—S552. http://dx.doi.org/10.21037/tcr.2019.07.24.

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18

Kumar, Manish, Indrajeet Kumar, Wasim Ahmed, et al. "Rare sites of giant cell tumor: Institutional experience." Journal of Indira Gandhi Institute Of Medical Sciences 7, no. 1 (2021): 12. http://dx.doi.org/10.4103/jigims.jigims_15_21.

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19

Mallick, Supriya, Soumyajit Roy, Rony Benson, Sudeep Das, P. K. Julka, and G. K. Rath. "Rare Sites of Metastasis From Gall Bladder Carcinoma." Journal of Gastrointestinal Cancer 46, no. 1 (2014): 74–76. http://dx.doi.org/10.1007/s12029-014-9674-z.

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20

Tan, W., and K. Wu. "Prostate cancer: biopsy proven rare sites of metastases." Journal of Clinical Oncology 23, no. 16_suppl (2005): 4794. http://dx.doi.org/10.1200/jco.2005.23.16_suppl.4794.

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21

Takahashi, Ei-ichi, Tada-aki Hori, and Motoi Murata. "Population cytogenetics of rare fragile sites in Japan." Human Genetics 78, no. 2 (1988): 121–26. http://dx.doi.org/10.1007/bf00278179.

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22

Hecht, F. "Rare, polymorphic, and common fragile sites: a classification." Human Genetics 74, no. 2 (1986): 207–8. http://dx.doi.org/10.1007/bf00282099.

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23

Pandit, S. K., K. N. Rattan, S. Budhiraja, and R. S. Solanki. "Cystic lymphangioma with special reference to rare sites." Indian Journal of Pediatrics 67, no. 5 (2000): 339–41. http://dx.doi.org/10.1007/bf02820682.

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24

Musio, Antonio, and Isabella Sbrana. "Common and rare fragile sites on human chromosomes." Cancer Genetics and Cytogenetics 88, no. 2 (1996): 184–85. http://dx.doi.org/10.1016/0165-4608(95)00287-1.

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25

Hecht, Frederick. "Minireview: Rare and polymorphic fragile sites and cancer." Cancer Genetics and Cytogenetics 34, no. 2 (1988): 195–99. http://dx.doi.org/10.1016/0165-4608(88)90259-2.

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26

Wang, Wenyan, Natalya V. Izarova, Jan van Leusen, and Paul Kögerler. "Polyoxometalates with separate lacuna sites." Chemical Communications 56, no. 94 (2020): 14857–60. http://dx.doi.org/10.1039/d0cc05791f.

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27

Thomakos, Nikolaos, Michail Diakosavvas, Nikolaos Machairiotis, Zacharias Fasoulakis, Paul Zarogoulidis, and Alexandros Rodolakis. "Rare Distant Metastatic Disease of Ovarian and Peritoneal Carcinomatosis: A Review of the Literature." Cancers 11, no. 8 (2019): 1044. http://dx.doi.org/10.3390/cancers11081044.

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Background: Although metastases of ovarian and peritoneal carcinomatosis are most commonly found within the peritoneal cavity, there is a number of other rare distant sites that have been reported. Our goal is to provide an evidence-based summary of the available literature considering the rare distant metastatic sites of ovarian and peritoneal carcinomatosis. Methods: A comprehensive search of the literature was conducted, with Medline/PubMed being searched for cases of rare metastatic disease originated from primary ovarian and peritoneal cancer with related articles up to 2019 including ter

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28

Guadagno, Elia, Gaetano De Rosa, and Marialaura Del Basso De Caro. "Neuroendocrine tumours in rare sites: differences in nomenclature and diagnostics—a rare and ubiquitous histotype." Journal of Clinical Pathology 69, no. 7 (2016): 563–74. http://dx.doi.org/10.1136/jclinpath-2015-203551.

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The diagnosis of neuroendocrine tumours in typical sites, as gastrointestinal tract and lung, is based upon well-coded criteria that have become familiar to most of the pathologists. Much more difficult is the recognition and allocation of proper nomenclature to be referred to the same histotype in locations where these tumours have a lower incidence. The aim of our review was to provide a quick handbook of the main diagnostic pitfalls known in literature that can interpose in the histopathological examination of neuroendocrine tumours in rare sites (urinary system and male genital organs, fem

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29

Mohanty, Arnab, and Debarghya Chatterjee. "A rare presentation of rectal endometriosis." International Surgery Journal 8, no. 3 (2021): 1066. http://dx.doi.org/10.18203/2349-2902.isj20210953.

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Endometriosis is the ectopic growth of viable endometrium outside the uterus, affecting approximately 7% women. It can occur in the absence of visible pelvic disease. Most common sites are gastrointestinal and urinary tract. Common sites of involvement are rectosigmoid (51%), appendix (15%), small bowel (14%), rectum (14%), cecum and colon (5%). Cyclical hematochezia is a definitive, but rare association of intestinal endometriosis. The diagnosis of colonic endometriosis is also difficult owing to the poor diagnostic yield of colonoscopy.

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30

Akkaya, Hampar, Bahar Akkaya, and Sinem Gonulcu. "Hydatid Disease Involving Some Rare Sites in the Body." Turkish Journal of Parasitology 39, no. 1 (2015): 78–82. http://dx.doi.org/10.5152/tpd.2015.3669.

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31

Sulabha, AN, S. Choudhari, and G. Suchitra. "Pyogenic granuloma - report of three cases in rare sites." Bangladesh Journal of Medical Science 12, no. 4 (2013): 445–48. http://dx.doi.org/10.3329/bjms.v12i4.16667.

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Pyogenic granuloma is a benign, localized mass of exuberant granulation tissue produced in response to various stimuli. It is inflammatory hyperplasia of oral cavity commonly seen on gingival area and rarely on other parts of oral cavity such as lips, tongue, palate and buccal mucosa. It is seen predominantly in 2nd to 3rd decade of life in young females. Clinically manifesting as small red erythematous exophytic lesion, it must be biopsied to rule out other serious conditions. This article aims to present three cases of extra gingival pyogenic granulomas occurring in rare sites such as buccal

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32

Sathe, PragatiAditya. "Lipoblastomas at rare sites: A report of two cases." Clinical Cancer Investigation Journal 10, no. 5 (2021): 267. http://dx.doi.org/10.4103/ccij.ccij_56_21.

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33

Cooke, D. W., B. L. Bennett, R. E. Muenchausen, K. J. McClellan, J. M. Roper, and M. T. Whittaker. "Intrinsic trapping sites in rare-earth and yttrium oxyorthosilicates." Journal of Applied Physics 86, no. 9 (1999): 5308–10. http://dx.doi.org/10.1063/1.371518.

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34

Loganathan, Karthik, Prabhu Vasudevan, Ajithkumar Krishnan, NawinSurya Aru-nachalam, and Akash Manivannan. "Solitary Osteochondroma in Uncommon Sites- A Rare Case Report." Journal of Orthopaedic Case Reports 15, no. 1 (2025): 166–70. https://doi.org/10.13107/jocr.2025.v15.i01.5164.

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Introduction: Osteochondroma is a bony lesion arising from the surface of the bone. It com-prises a large percentage of all benign bone tumors. A unique feature of this tumor is the conti-nuity of cortical and medullary components between the normal bony tissue and aberrant tissue of osteochondroma. Even though the predominant composition is bone, growth takes place in the cartilaginous portion. The incidence of osteochondroma in flat bones which are ossified by intramembranous type of ossification including the scapula, clavicle, ribs, and pubic ramus is usually rare. Case Report: We report t

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35

Chawla, A., D. Mishra, R. Bansal, and M. Chundru. "Rare sites of delayed metastasis in renal cell carcinoma." Case Reports 2013, jun21 1 (2013): bcr2013009971. http://dx.doi.org/10.1136/bcr-2013-009971.

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36

Benmeir, P., A. Baruchin, A. Weinberg, O. Nahlieli, A. Neuman, and M. R. Wexler. "Rare sites of melanoma: melanoma of the external ear." Journal of Cranio-Maxillofacial Surgery 23, no. 1 (1995): 50–53. http://dx.doi.org/10.1016/s1010-5182(05)80256-2.

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37

Colpa, J. H. P., P. H. Frings, R. J. Radwański, J. J. M. Franse, and M. Alba. "Molecular field at the rare-earth sites in Nd2Co17." Journal of Magnetism and Magnetic Materials 131, no. 1-2 (1994): 167–72. http://dx.doi.org/10.1016/0304-8853(94)90024-8.

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38

Schwartz, Michal, Eitan Zlotorynski, and Batsheva Kerem. "The molecular basis of common and rare fragile sites." Cancer Letters 232, no. 1 (2006): 13–26. http://dx.doi.org/10.1016/j.canlet.2005.07.039.

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39

Kähkönen, M., J. Leisti, C. J. Thoden, and S. Autio. "Frequency of rare fragile sites among mentally subnormal schoolchildren." Clinical Genetics 30, no. 3 (2008): 234–38. http://dx.doi.org/10.1111/j.1399-0004.1986.tb00601.x.

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40

Côté, Gilbert B. "The cis-configuration effects of rare chromosomal fragile sites." Clinical Genetics 37, no. 6 (2008): 470–72. http://dx.doi.org/10.1111/j.1399-0004.1990.tb03532.x.

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41

Muni Muralidhar Rao, Kommanagunta, and K. Usha Sree. "RARE PRSENTATION OF GIANT CELL TUMOR AT UNUSUAL SITES." International Journal of Advanced Research 7, no. 10 (2019): 944–54. http://dx.doi.org/10.21474/ijar01/9913.

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42

Adam, Sanda, Gh Adam, and E. Burzo. "Crystal fields at rare-earth sites in R2Fe14B compounds." Journal of Magnetism and Magnetic Materials 61, no. 3 (1986): 260–66. http://dx.doi.org/10.1016/0304-8853(86)90036-3.

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43

Samadder, Pranati, Jane A. Evans, and Albert E. Chudley. "Segregation analysis of rare autosomal folate sensitive fragile sites." American Journal of Medical Genetics 46, no. 2 (1993): 165–71. http://dx.doi.org/10.1002/ajmg.1320460213.

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44

Shalata, Walid, Ashraf Abu Jama, Amjad Abu Salman, et al. "Unexpected and Rare Sites of Metastasis in Oncologic Patients." Journal of Clinical Medicine 12, no. 20 (2023): 6447. http://dx.doi.org/10.3390/jcm12206447.

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Case studies of rare oncologic metastases are an important source of clinical data for health care professionals and researchers. While infrequent, the knowledge base and clinical recommendations derived from such cases aid in advancements in the field. As such, we aim to add five cases to the growing body of literature. The first two male patients, aged 69 and 73, were diagnosed with colon adenocarcinoma, suspected to be a second primary prostate carcinoma, following positron emission tomography-computer tomography (PET-CT). This suspicion was ruled out by prostatectomy and histopathological

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45

Zlotorynski, Eitan, Ayelet Rahat, Jennifer Skaug, et al. "Molecular Basis for Expression of Common and Rare Fragile Sites." Molecular and Cellular Biology 23, no. 20 (2003): 7143–51. http://dx.doi.org/10.1128/mcb.23.20.7143-7151.2003.

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ABSTRACT Fragile sites are specific loci that form gaps, constrictions, and breaks on chromosomes exposed to partial replication stress and are rearranged in tumors. Fragile sites are classified as rare or common, depending on their induction and frequency within the population. The molecular basis of rare fragile sites is associated with expanded repeats capable of adopting unusual non-B DNA structures that can perturb DNA replication. The molecular basis of common fragile sites was unknown. Fragile sites from R-bands are enriched in flexible sequences relative to nonfragile regions from the

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46

Rastogi, N., R. K. Singh, and N. Rai. "Primary bilateral leiomyosarcoma of kidneys with metastases at unusual sites- a rare case report." Asian Pacific Journal of Health Sciences 3, no. 2 (2016): 16–18. http://dx.doi.org/10.21276/apjhs.2016.3.2.4.

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47

Martinelli, Ida, Massimo Franchini, and Pier Mannuccio Mannucci. "How I treat rare venous thromboses." Blood 112, no. 13 (2008): 4818–23. http://dx.doi.org/10.1182/blood-2008-07-165969.

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Abstract Venous thromboembolism may involve venous sites other than the lower limbs, such as cerebral, splanchnic, and upper limb veins. Although uncommon, these thromboses may be clinically severe and challenging for caregivers. In this review, the main pathogenic, clinical, and therapeutic features of thromboses in rare venous sites are discussed. Even though there was a lot of recent progress in understanding the mechanistic role of inherited and acquired thrombophilia and of the interactions between different risk factors, the optimal management of these patients is still unsettled, being

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48

Dowell, Erika. "Web Site Usability for Rare Book and Manuscript Libraries." RBM: A Journal of Rare Books, Manuscripts, and Cultural Heritage 9, no. 2 (2008): 168–82. http://dx.doi.org/10.5860/rbm.9.2.306.

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The information presented on the Web sites of special collections libraries is often very different from the information included on the Web sites of general collections libraries. Descriptions of manuscripts, finding aids in HTML or PDF formats, Encoded Archival Description findings aids, short-title lists, and home-grown databases are among the diverse resources that may be found on Web sites of special collections libraries. Additionally, the Web site may be required to describe certain important sources of information that are not available online, such as finding aids in hard copy or a ca

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49

Martin-Trujillo, Alejandro, Nihir Patel, Felix Richter, et al. "Rare genetic variation at transcription factor binding sites modulates local DNA methylation profiles." PLOS Genetics 16, no. 11 (2020): e1009189. http://dx.doi.org/10.1371/journal.pgen.1009189.

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Although DNA methylation is the best characterized epigenetic mark, the mechanism by which it is targeted to specific regions in the genome remains unclear. Recent studies have revealed that local DNA methylation profiles might be dictated by cis-regulatory DNA sequences that mainly operate via DNA-binding factors. Consistent with this finding, we have recently shown that disruption of CTCF-binding sites by rare single nucleotide variants (SNVs) can underlie cis-linked DNA methylation changes in patients with congenital anomalies. These data raise the hypothesis that rare genetic variation at

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50

Gashi, Zaim, Astrit Hamza, Blerina Ukimeri, Valon Hamza, and Marigona Zubaku-Rakovic. "A Rare Case of Gastric Metastasis from a Rare Case of Mucosal Malignant Melanoma." Open Access Macedonian Journal of Medical Sciences 12, no. 2 (2024): 362–64. http://dx.doi.org/10.3889/oamjms.2024.11917.

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BACKGROUND: Malignant melanoma (MM) is the deadliest form of skin cancer and the most common carcinoma to metastasize into the gastrointestinal tract (GI). While the jejunum, ileum, colon, and rectum are common gastrointestinal sites of metastasis, metastatic melanoma in the stomach is rare and usually not detected until late in the disease. CASE PRESENTATION: We report a patient who presented with hematemesis, epigastric pain, and weight loss. In the second esophagogastroduodenoscopy, after 8 months from the first endoscopic assessment, a double ulcerative gastric mass was found, and histopat

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