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1 part reflects the high prevalence of benign adnexal abnormalities and the more frequent detection of
8 showed differential expression in epidermal, adnexal, and corneal epithelia but were not significantl
9 nical and histopathologic findings of ocular adnexal angiolymphoid hyperplasia with eosinophilia, an
11 ejection, such as skin stricture, hair loss, adnexal atrophy, extensive fibrosis and mast cell infilt
13 spasm who were consecutively recruited from adnexal clinics at Moorfields Eye Hospital (January-June
15 tients regarding the benign nature of simple adnexal cysts after a diagnostic-quality US examination
17 f malignancy in incidentally detected simple adnexal cysts at computed tomography (CT) to determine i
18 clusion The prevalence of previously unknown adnexal cysts at CT was 6.6%, with an ovarian cancer rat
21 e interpreting radiologists' reports for 398 adnexal cysts detected at ultrasonography in 398 patient
22 etrospective review was performed, including adnexal cysts detected with ultrasonography (US) with su
24 egarding the management of ovarian and other adnexal cysts imaged sonographically in asymptomatic wom
26 sts in Ultrasound (SRU) guidelines on simple adnexal cysts with recent large studies showing exceptio
31 demonstrate that C. psittaci-negative ocular adnexal EMZL exhibit biased usage of IGHV families and g
35 nuckle skin was weak or absent, although its adnexal expression appeared normal and the punctate memb
36 an cancer developed subsequent to a negative adnexal finding at CT examination during a 15-44-month i
38 rent studies, WNV infected the epidermis and adnexal glands of mouse skin, and the epidermal cells we
40 nic mice reported here exhibit epidermal and adnexal hyperplasia, hyperkeratosis, and almost total al
42 y and includes a diverse group of experts on adnexal imaging and management who developed the O-RADS
43 kelihood of cancer; and future directions of adnexal imaging for the early detection of ovarian cance
44 -solving tool through the use of the Ovarian-Adnexal Imaging Reporting and Data System (O-RADS) MRI l
49 Eighteen cases of ocular surface or ocular adnexal invasive squamous cell carcinomas were identifie
51 id hyperplasia with eosinophilia with ocular adnexal involvement are variable and include eyelid swel
52 Dacryoadenitis is the rarest form of ocular adnexal involvement in regional enteritis, which affects
54 f malignancy based on the MRI features of an adnexal lesion and provides information to facilitate op
59 scoring system in a cohort of indeterminate adnexal lesions according to International Ovarian Tumor
60 ion systems to characterize US-indeterminate adnexal lesions and of the category-wise malignancy rate
61 odels can help nonexpert clinicians evaluate adnexal lesions and reduce surgical interventions for be
62 ic contrast-enhanced MRI scans to categorize adnexal lesions as benign or malignant and to evaluate t
63 mptoms who underwent surgery for ovarian and adnexal lesions before the O-RADS US risk score was publ
64 dy of women undergoing MRI for indeterminate adnexal lesions between March 2013 and March 2018, was q
68 his article will review how the treatment of adnexal lesions has changed due to imaging over the deca
71 he inclusion of imaging in the evaluation of adnexal lesions in the 1970s, the rate of surgery for be
76 n schema of classic- or nonclassic-appearing adnexal lesions resulted in high sensitivity and specifi
80 ) ages of patients with benign and malignant adnexal lesions were 44.1 (14.4) and 52.5 (15.2) years,
82 mean age, 53.2 years +/- 16.3 [SD]) with 372 adnexal lesions were included: 10 reports in the trainin
85 002, to July 24, 2012, 74 cystic hemorrhagic adnexal lesions with hyperintense signal on T1-weighted
86 e the proportion of patients with ovarian or adnexal lesions without acute symptoms who may have been
88 system for characterization of indeterminate adnexal lesions, a non-negligible percentage of adnexal
89 vides a standardized lexicon for ovarian and adnexal lesions, enables stratification of these lesions
90 atification of sonographically indeterminate adnexal lesions, partly based on time-intensity curve (T
92 s the initial modality for the assessment of adnexal lesions, while MRI is used when there is a clini
93 MRI systems to characterize US-indeterminate adnexal lesions, with pathologic examination and/or foll
103 differentiating between benign and malignant adnexal lesions; this outcome has been previously report
104 s year, advances in the management of ocular adnexal lymphoid tumors have been based on the distincti
105 in patients with a prior diagnosis of ocular adnexal lymphoma (OAL) and to determine latency periods
106 efficacy of available treatments for ocular adnexal lymphoma (OAL) and to evaluate the outcomes and
107 features of the follicular subtype of ocular adnexal lymphoma (OAL) have not been previously evaluate
108 ge B-cell lymphoma (DLBCL) subtype of ocular adnexal lymphoma have not previously been evaluated in a
110 Patients with prior diagnosis of ocular adnexal lymphoma possess increased risk of hematologic a
111 urrent systemic lymphoma (29.0%), and ocular adnexal lymphoma relapse of previous systemic lymphoma (
113 ing for up to 80% of cases of primary ocular adnexal lymphoma, is marginal zone lymphoma of mucosa-as
120 ed in the management of patients with ocular adnexal MALT lymphoma, especially monoclonal antibody th
121 s have been adequately tested only in ocular adnexal MALT lymphomas where upfront doxycycline may be
123 r knowledge, the clinical features of ocular adnexal mantle-cell lymphoma (OA-MCL) have not previousl
124 tween Chlamydophila psittaci (Cp) and ocular adnexal marginal zone lymphoma (OAMZL) and the efficacy
125 f the screening cohort, had an indeterminate adnexal mass (108 unilateral, 10 bilateral; mean size, 4
126 mination for the exploration of an equivocal adnexal mass (January 2007 to December 2012) with surgic
127 ness (LR+ 4.9; 95% CI, 1.7-14; n = 1435), an adnexal mass (LR+ 2.4; 95% CI, 1.6-3.7; n = 1378), and a
129 onsecutive adult patients presenting with an adnexal mass between January 1, 2012, and March 1, 2015,
130 included 4905 patients with a newly detected adnexal mass in 17 centers that met predefined data qual
132 e selected for conservative management of an adnexal mass judged to be benign on ultrasound on the ba
134 nts aged 18 years or older with at least one adnexal mass who had been selected for surgery or conser
140 ith ovarian cancer are for the evaluation of adnexal masses and for the diagnosis and evaluation of r
141 an also be helpful in characterizing complex adnexal masses and in depicting recurrent tumor after tr
143 rian Tumor Analysis) Simple Rules classifies adnexal masses as benign, malignant, or indeterminate ba
145 lded 54 patients with breast cancer and with adnexal masses at US and histopathologic examinations.
146 ive women with sonographically indeterminate adnexal masses between November 2016 and December 2018.
148 nts, and supports conservative management of adnexal masses classified as benign by use of ultrasound
150 during the first 2 years of follow-up after adnexal masses have been classified as benign by use of
151 independently reviewed the sonograms of 252 adnexal masses in 226 women and recorded US features by
152 differentiating between benign and malignant adnexal masses is proportional to the expertise of the o
153 pian tubes and differentiate them from other adnexal masses on the basis of morphologic features.
155 onsecutive patients aged 18 to 89 years with adnexal masses that were managed surgically or conservat
157 cale and Doppler sonographic features of 211 adnexal masses were correlated with the final diagnosis;
159 malignancy and acute complications is low if adnexal masses with benign ultrasound morphology are man
160 ging features that had been recorded for the adnexal masses with each imaging modality were reviewed
161 rospective study of sonographically detected adnexal masses with known clinical outcomes from two ins
163 ning risk of malignancy to ovarian and other adnexal masses, and to provide a management recommendati
164 set of 38 patients with surgically evaluated adnexal masses, but no hydrosalpinx, were randomly chose
165 more accurate and consistent evaluations of adnexal masses, especially when used by nonexpert clinic
166 lipid metabolic phenotypes in patients with adnexal masses, integrating quantitative lipidomics prof
167 n the evaluation of the pregnant patient for adnexal masses, pelvimetry, hydroureteronephrosis of pre
169 nhanced MR imaging depicted 176 (94%) of 187 adnexal masses, with an overall accuracy for the diagnos
170 he detection and characterization of complex adnexal masses, with excellent inter- and intraobserver
177 Fifty-five patients were included; ocular adnexal MCL was found to be most common in older individ
181 lator of NF-kappaB, were described in ocular adnexal MZL, suggesting a role for A20 as a tumor suppre
182 orders and whether it differs between ocular adnexal MZLs with (IgG4-associated MZL) and without (IgG
184 ool database, 4.5% of feline intraocular and adnexal neoplasms (234/5153) were designated as feline o
185 dentified as potential aggravators of ocular adnexal neoplasms; however, given the rarity of these ne
186 erapy and radioimmunotherapy for orbital and adnexal non-Hodgkin's lymphoma and other lymphoprolifera
189 The results demonstrate that the ocular and adnexal organs function as a unified visual system, with
196 assess interreader agreement of the Ovarian-Adnexal Reporting and Data System (O-RADS) and intermoda
201 sion Pelvic MRI interpreted with the Ovarian-Adnexal Reporting and Data System (O-RADS) MRI lexicon h
202 diffusion-weighted imaging (DWI) to Ovarian-Adnexal Reporting and Data System (O-RADS) MRI to improv
203 l lesions can be stratified into the Ovarian-Adnexal Reporting and Data System (O-RADS) risk of malig
205 American College of Radiology (ACR) Ovarian-Adnexal Reporting and Data System (O-RADS) ultrasound (U
210 rtiary referral oncology center, the Ovarian-Adnexal Reporting and Data System US risk stratification
214 acrimal gland and primary orbital and ocular adnexal soft tissue tumors; reappraisal of diagnostic, p
215 s to update ophthalmologists and orbital and adnexal specialists with the emerging role of targeted m
216 ic-pathologic correlation was performed with adnexal specimens imaged in vitro in three study patient
217 other organs, just the aging of skin and its adnexal structure the hair follicle can result in cosmet
219 s residing close to the surface and includes adnexal structures and present data showing that tape an
220 ncreased complexity that better mimic native adnexal structures can have a substantial impact on rege
221 on also restored skin architecture including adnexal structures in ear wounds and dermal-epidermal ju
224 was associated with atrophy of epidermal and adnexal structures of skin; a similar phenotype is repor
225 gment our PS-OCT measurements by visualizing adnexal structures such as hair follicles to relay overa
226 roaches fail to adequately introduce complex adnexal structures such as hair follicles within tissue
228 Initial development of the skin's epidermis, adnexal structures, and barrier function is necessary fo
232 ss (LR+ 2.4; 95% CI, 1.6-3.7; n = 1378), and adnexal tenderness (LR+ 1.9; 95% CI, 1.0-3.5; n = 1435)
234 r diseases that involve the orbit and ocular adnexal tissue, such as lymphoma, hemangioma, sarcoidosi
236 s an accurate technique for the diagnosis of adnexal torsion in patients who have an adnexal mass wit
238 l: 1.2, 56.8], P = .03) were associated with adnexal torsion, with substantial interreader agreement
240 sts who had managed, on average, 52 globe or adnexal trauma cases throughout their careers and/or pub
243 onths, 34 (28%) patients developed no ocular/adnexal tumor, 86 (72%) developed ocular surface maligna
246 udy investigates the role of TKTL1 in ocular adnexal tumors and analyzes how its expression correlate
248 ognostic, and therapeutic approach to ocular adnexal tumors in light of emerging molecular genetic da
250 radenoma and cylindroma are distinctive skin adnexal tumors with sweat gland differentiation and pote
255 d anti-Yo antibody response in whom ovarian, adnexal, uterine, or breast cancer cannot be detected.