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Articoli di riviste sul tema "Distinct entity"

Autore: Grafiati

Pubblicato: 13 aprile 2024

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1

Husein El Ahmed, Husein, and Carmen Dulanto-Campos. "A distinct entity." American Journal of Obstetrics and Gynecology 208, no. 1 (2013): 89.e1–89.e2. http://dx.doi.org/10.1016/j.ajog.2012.10.864.

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2

Gleich, Tobias, Elena Chiticariu, Marcel Huber, and Daniel Hohl. "Keratoacanthoma: a distinct entity?" Experimental Dermatology 25, no. 2 (2015): 85–91. http://dx.doi.org/10.1111/exd.12880.

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3

Grof, Paul. "Melancholia: A Distinct Entity?" Canadian Journal of Psychiatry 58, no. 4 (2013): 181–82. http://dx.doi.org/10.1177/070674371305800401.

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4

H. Khaparde, Sadhana, Sanjay D. Deshmukh, Baba B. Shinde, Prajacta Rane, and Shaleen Lamba. "Sialadenoma Papilliferum of Buccal Mucosa : A Rare and Distinct Entity." Indian Journal of Pathology: Research and Practice 5, no. 2 (2016): 219–21. http://dx.doi.org/10.21088/ijprp.2278.148x.5216.28.

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5

Agarwal, Amar, Priya Narang, and DhivyaAshok Kumar. "Predescemetocele: A distinct clinical entity." Indian Journal of Ophthalmology 65, no. 11 (2017): 1224. http://dx.doi.org/10.4103/ijo.ijo_492_17.

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6

Bomback, Andrew S., and Glen S. Markowitz. "Lupus Podocytopathy: A Distinct Entity." Clinical Journal of the American Society of Nephrology 11, no. 4 (2016): 547–48. http://dx.doi.org/10.2215/cjn.01880216.

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7

Joshi, Rajiv, and Yatin Jadhav. "Penoscrotal porokeratosis: A distinct entity." Indian Dermatology Online Journal 6, no. 5 (2015): 339. http://dx.doi.org/10.4103/2229-5178.164487.

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8

Levine, Jimmy, Michael H. Schmidt, Morton I. Burrell, and Michael S. Hopkins. "Acute Jejunoileitis. A Distinct Entity?" Journal of Clinical Gastroenterology 14, no. 1 (1992): 47–51. http://dx.doi.org/10.1097/00004836-199201000-00012.

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9

Walters, Glenn D. "Dementia: Continuum or distinct entity?" Psychology and Aging 25, no. 3 (2010): 534–44. http://dx.doi.org/10.1037/a0018167.

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10

McMillan, Marcia J., and R. O. Pihl. "Premenstrual depression: A distinct entity." Journal of Abnormal Psychology 96, no. 2 (1987): 149–54. http://dx.doi.org/10.1037/0021-843x.96.2.149.

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11

Dixon, M. F., H. J. O'Connor, A. T. Axon, R. F. King, and D. Johnston. "Reflux gastritis: distinct histopathological entity?" Journal of Clinical Pathology 39, no. 5 (1986): 524–30. http://dx.doi.org/10.1136/jcp.39.5.524.

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12

Pranteda, Bottoni, De Simone, Calvieri, and Grieco. "Bullous keloid: a distinct entity?" British Journal of Dermatology 141, no. 2 (1999): 375–77. http://dx.doi.org/10.1046/j.1365-2133.1999.03013.x.

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13

Yazıcı, Olcay. "Unipolar mania: A distinct entity?" Journal of Affective Disorders 152-154 (January 2014): 52–56. http://dx.doi.org/10.1016/j.jad.2013.10.005.

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14

Amarapurkar, Anjali D., Deepak Amarapurkar, Mehul Choksi, Nirav Bhatt, and Pooja Amarapurkar. "Portal hypertensive polyps: distinct entity." Indian Journal of Gastroenterology 32, no. 3 (2013): 195–99. http://dx.doi.org/10.1007/s12664-013-0324-3.

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15

Ammann, Roland A., Jack Plaschkes, and Kurt Leibundgut. "Congenital hepatoblastoma: A distinct entity?" Medical and Pediatric Oncology 32, no. 6 (1999): 466–68. http://dx.doi.org/10.1002/(sici)1096-911x(199906)32:6<466::aid-mpo20>3.0.co;2-1.

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16

Korelitz, Burton I., та Jeffrey Aronoff. "Crohnʼs proctitis: A distinct entity". Inflammatory Bowel Diseases 16, № 5 (2010): 721–22. http://dx.doi.org/10.1002/ibd.21089.

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17

Hennekam, R. C. M. "LADD syndrome: a distinct entity?" European Journal of Pediatrics 146, no. 1 (1987): 94–95. http://dx.doi.org/10.1007/bf00647303.

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18

LEVINSON, JOSEPH E. "Eosinophilic Fasciitis: A Distinct Entity?" Archives of Pediatrics & Adolescent Medicine 139, no. 1 (1985): 8. http://dx.doi.org/10.1001/archpedi.1985.02140030010001.

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19

Garg, RavindraKumar, GyanPrakash Singh, Rajiv Garg, Neeraj Kumar, and Anit Parihar. "Severe COVID-19: A distinct entity." Journal of Family Medicine and Primary Care 10, no. 1 (2021): 84. http://dx.doi.org/10.4103/jfmpc.jfmpc_1600_20.

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20

Pawar, Vipul Mohan. "Verruciform Xanthoma-Histopathologically: A Distinct Entity." Journal of Contemporary Dentistry 4, no. 3 (2014): 181–84. http://dx.doi.org/10.5005/jp-journals-10031-1093.

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Abstract (sommario):

ABSTRACT Verruciform xanthoma (VX) is an uncommon benign mucocutaneous lesion of unknown etiology. It is essential to diagnose this lesion as a varied entity of utmost importance as clinically their appearance could range from a simple leukoplakia or papilloma to as grave as squamous cell carcinoma SCC. Although this lesion is of multifactorial pathogenesis, a viral etiology like human papilloma virus (HPV) has been suggested in some cases. This rare, harmless lesion usually presents as a sessile or pedunculated, pale yellowish-to-red, papillary, granular or verrucous mucosal growth. Histopathologically, VX is characterized by the presence of parakeratinzed epithelium showing papillary or verrucous growth with thin rete ridges and connective tissue papillae extending up to the surface. The papillae characteristically consist of foam cells, also called xanthoma cells. We report two cases of VX of varied clinical appearance but very similar and characteristic histopathological presentation to be diagnosed as VX. The clinical diagnosis, though may be challenging; the histopathological features are diagnostic and well-defined. It is also noteworthy that in an improper biopsy, xanthoma cells may be scanty and their presence can be missed, especially if one is unfamiliar with the existence of this lesion. How to cite this article Pawar VM, Patel S, Pathak J, Swain N. Verruciform Xanthoma-Histopathologically: A Distinct Entity. J Contemp Dent 2014;4(3):181-184.

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21

Ray, Katrina. "Eosinophilic colitis — a distinct clinical entity?" Nature Reviews Gastroenterology & Hepatology 19, no. 3 (2022): 148. http://dx.doi.org/10.1038/s41575-022-00583-0.

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22

Kansal, NaveenKumar, C. Divyalakshmi, and Aditi Dhanta. "Lichenoid psoriasis: A distinct morphological entity." Clinical Dermatology Review 4, no. 1 (2020): 67. http://dx.doi.org/10.4103/cdr.cdr_15_19.

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23

Morris, Gabrielle F., Katrina Murphy, Lucy B. Rorke, and Hector E. James. "Spinal hamartomas: a distinct clinical entity." Journal of Neurosurgery 88, no. 6 (1998): 954–61. http://dx.doi.org/10.3171/jns.1998.88.6.0954.

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Abstract (sommario):

Object. Congenital spinal hamartomas are defined as tumors of well-differentiated mature elements situated in an abnormal location. In this report, the authors document the clinical and pathological features of spinal hamartomas in 10 patients. Methods. Ten patients presented with midline dorsal malformations at birth, initially diagnosed as teratomas or myelomeningoceles. The locations of the masses were variable: two were located in the thoracic region, four at the thoracolumbar junction, two in the lumbar region, one at the lumbosacral junction, and one in the sacral region. The results of the neurological examination were normal in nine patients. All but one mass had intact skin and seven had palpable bone components. Neuroimaging studies revealed widening of the spinal canal, heterotopic bone located dorsally in some patients, and varying degrees of involvement of the intraspinal contents. During surgery, six patients were found to have involvement of the spinal cord or cauda equina. The pathological characteristics of the masses included three or more of the following: bone, cartilage, synovial membrane, urinary tract tissue, cyst wall, yellow or brown fat, and nerves. The well-differentiated cellular elements, which formed mature structures, along with the absence of primitive cellular components and neoplastic characteristics are more consistent with a diagnosis of hamartoma than teratoma. Conclusions. In this series, the authors describe a lesion that is overt on physical examination, yet can have occult spinal canal involvement. Complete neurosurgical evaluation is essential to provide appropriate treatment and prognosis.

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24

Wasserfallen, Jean-Blaise, Marie-Denise Schaller, Francois Feihl, and Claude H. Perret. "Sudden Asphyxic Asthma: A Distinct Entity?" American Review of Respiratory Disease 142, no. 1 (1990): 108–11. http://dx.doi.org/10.1164/ajrccm/142.1.108.

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25

Strong, Russell W. "DIEULAFOY'S DISEASE-A DISTINCT CLINICAL ENTITY." Australian and New Zealand Journal of Surgery 54, no. 4 (2008): 337–39. http://dx.doi.org/10.1111/j.1445-2197.1984.tb05329.x.

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26

Sabatelli, M., F. Madia, L. De Armas, and P. Tonali. "PURE MOTOR CIDP. A DISTINCT ENTITY?" Journal of the Peripheral Nervous System 5, no. 1 (2000): 49. http://dx.doi.org/10.1046/j.1529-8027.2000.00513-52.x.

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27

FLETCHER, C. D. M., S. E. DAVIES, and P. H. MCKEE. "Cellular schwannoma: a distinct pseudosarcomatous entity." Histopathology 11, no. 1 (2007): 21–35. http://dx.doi.org/10.1111/j.1365-2559.1987.tb02606.x.

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28

Gertz, Morie A., Francis K. Buadi, Suzanne R. Hayman, et al. "Immunoglobulin D amyloidosis: a distinct entity." Blood 119, no. 1 (2012): 44–48. http://dx.doi.org/10.1182/blood-2011-06-358895.

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Abstract IgD monoclonal gammopathies are uncommon. They are seen rarely as a monoclonal gammopathy of undetermined significance and are present in 1%-2% of patients with multiple myeloma. In light-chain amyloidosis, IgD monoclonal proteins are found in ap-proximately 1% of patients. When an IgD monoclonal protein is found, amyloidosis is often omitted from the differential diagnosis. In the present study, we reviewed the natural history of IgD-associated amyloidosis among 53 patients seen over 41 years. The distribution of clinical syndromes suggests that these patients have a lower frequency of renal and cardiac involvement. The overall survival of these patients does not appear to be different from that of patients who have light-chain amyloidosis associated with another monoclonal protein.

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29

van der Meijden, Willem I., and Patricia C. Ewing. "Papular Colpitis: A Distinct Clinical Entity?" Journal of Lower Genital Tract Disease 15, no. 1 (2011): 60–65. http://dx.doi.org/10.1097/lgt.0b013e3181dc2f6a.

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30

Amarapurakar, Deepak, Anjali D. Amarapurkar, Nirav Bhatt, Mehul J. Choksi, and Pooja Amarapurkar. "Su1959 Portal Hypertensive Polyps: Distinct Entity." Gastroenterology 142, no. 5 (2012): S—546. http://dx.doi.org/10.1016/s0016-5085(12)62098-8.

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31

Oliver, G. Fergus, and R. K. Winkelmann. "Unilesional mycosis fungoides: A distinct entity." Journal of the American Academy of Dermatology 20, no. 1 (1989): 63–70. http://dx.doi.org/10.1016/s0190-9622(89)70008-6.

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32

Smith, Dr Molly, Dr Craig Fowler, Dr Indraneel Bhattacharyya, Dr Rekha Reddy, and Dr Douglas Damm. "AMELOBLASTIC fiBRO-ODONTOMA: A DISTINCT ENTITY." Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology 128, no. 1 (2019): e89. http://dx.doi.org/10.1016/j.oooo.2019.02.227.

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33

Dhondt, E., L. Oudenhoven, S. Khan, et al. "Nora’s lesion, a distinct radiological entity?" Skeletal Radiology 35, no. 7 (2006): 497–502. http://dx.doi.org/10.1007/s00256-005-0041-9.

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34

Hyser, Craig L., John T. Kissel, John R. Warmolts, and Jerry R. Mendell. "Scapuloperoneal neuropathy: A distinct clinicopathologic entity." Journal of the Neurological Sciences 87, no. 1 (1988): 91–102. http://dx.doi.org/10.1016/0022-510x(88)90057-3.

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35

Mori, Makoto, Robert W. Elder, and Wendy M. Book. "Adult Fontan failure — Distinct disease entity." International Journal of Cardiology 177, no. 2 (2014): 650. http://dx.doi.org/10.1016/j.ijcard.2014.09.177.

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36

Krutchkoff, David J., and Ellen Eisenberg. "Lichenoid dysplasia: A distinct histopathologic entity." Oral Surgery, Oral Medicine, Oral Pathology 60, no. 3 (1985): 308–15. http://dx.doi.org/10.1016/0030-4220(85)90315-9.

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37

Bitton, Rachelle N., and Craig Wexler. "Free triiodothyronine toxicosis: A distinct entity." American Journal of Medicine 88, no. 5 (1990): 531–33. http://dx.doi.org/10.1016/0002-9343(90)90435-g.

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38

Sakata, Shigeki, and Toru Ogawa. "Free T3 toxicosis: A distinct entity?" American Journal of Medicine 91, no. 1 (1991): 100. http://dx.doi.org/10.1016/0002-9343(91)90083-a.

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39

Behranwala, K. A., and J. M. Thomas. "‘Aggressive’ angiomyxoma: a distinct clinical entity." European Journal of Surgical Oncology (EJSO) 29, no. 7 (2003): 559–63. http://dx.doi.org/10.1016/s0748-7983(03)00104-5.

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40

Van Borsel, John, Sandie Van Der Made, and Patrick Santens. "Thalamic stuttering: A distinct clinical entity?" Brain and Language 85, no. 2 (2003): 185–89. http://dx.doi.org/10.1016/s0093-934x(03)00061-0.

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41

Weatherald, Jason, Peter Dorfmüller, Frédéric Perros, et al. "Pulmonary capillary haemangiomatosis: a distinct entity?" European Respiratory Review 29, no. 156 (2020): 190168. http://dx.doi.org/10.1183/16000617.0168-2019.

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Abstract (sommario):

Pulmonary capillary haemangiomatosis (PCH) is a rare and incompletely understood histopathological finding characterised by abnormal capillary proliferation within the alveolar interstitium, which has long been noted to share many overlapping features with pulmonary veno-occlusive disease (PVOD). But are PCH and PVOD distinct entities that occur in isolation, or are they closely intertwined manifestations along a spectrum of the same disease? The classic clinical features of both PCH and PVOD include signs and symptoms related to pulmonary hypertension, hypoxaemia, markedly impaired diffusion capacity of the lung and abnormal chest imaging with ground glass opacities, septal lines and lymphadenopathy. In recent years, increasing evidence suggests that the clinical presentation, histopathological features, genetic substrate and pathobiological mechanisms of PCH and PVOD are overlapping and usually indistinguishable. The discovery of biallelic mutations in the eukaryotic translation initiation factor 2 α kinase 4 (EIF2AK4) gene in heritable PCH and PVOD greatly advanced our understanding of the overlapping nature of these conditions. Furthermore, recognition of PCH and PVOD-like changes in other pulmonary vascular diseases and in conditions that cause chronic pulmonary venous hyper-perfusion or hypertension suggests that PCH/PVOD may develop as a reactive process to various insults or injuries to the pulmonary vasculature, rather than being primary angiogenic disorders.

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42

Steensma, David P., Curtis A. Hanson, Louis Letendre, and Ayalew Tefferi. "Myelodysplasia with fibrosis: a distinct entity?" Leukemia Research 25, no. 10 (2001): 829–38. http://dx.doi.org/10.1016/s0145-2126(01)00055-8.

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43

Durrani, Khayyam, and C. Stephen Foster. "Psoriatic uveitis: A distinct clinical entity?" American Journal of Ophthalmology 139, no. 1 (2005): 106–11. http://dx.doi.org/10.1016/j.ajo.2004.08.053.

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44

Mackworth-Young, Charles. "Primary antiphospholipid syndrome: A distinct entity?" Autoimmunity Reviews 5, no. 1 (2006): 70–75. http://dx.doi.org/10.1016/j.autrev.2005.08.001.

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45

Cohen, Pierre Alain, G. Kalifa, Veronica Donoghue, Catherine Adamsbaum, Faddy Haddad, and Jean Dubousset. "Ischio-vertebral dysplasia: a distinct entity." Pediatric Radiology 29, no. 2 (1999): 131–34. http://dx.doi.org/10.1007/s002470050556.

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46

Shin, Jung-Ha, Tae-Eun Kim, Kyo-Young Lee, Sang-In Shim, and Yeong-Jin Choi. "C1q Nephropathy: A Distinct Pathologic Entity." Korean Journal of Pathology 43, no. 4 (2009): 335. http://dx.doi.org/10.4132/koreanjpathol.2009.43.4.335.

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47

Kumar, Bhushan, and Davinder Parsad. "Is ‘Nodular Tuberculid’ A Distinct Entity?" Pediatric Dermatology 18, no. 2 (2001): 165–66. http://dx.doi.org/10.1046/j.1525-1470.2001.01894-3.x.

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48

Kokal, William A., L. Robert Hill, David Porudominsky, et al. "Inflammatory breast carcinoma: A distinct entity?" Journal of Surgical Oncology 30, no. 3 (2006): 152–55. http://dx.doi.org/10.1002/jso.2930300306.

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49

Roach, E. S. "Is Neuromyelitis Optica a Distinct Entity?" Archives of Neurology 64, no. 6 (2007): 906. http://dx.doi.org/10.1001/archneur.64.6.906.

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50

Gulia, Joyti, Shambu Aryal, Haval Saadlla, and Andrew F. Shorr. "Healthcare-associated candidemia-A distinct entity?" Journal of Hospital Medicine 5, no. 5 (2010): 298–301. http://dx.doi.org/10.1002/jhm.652.

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