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1.
Oman J Ophthalmol ; 11(3): 254-258, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30505117

RESUMO

AIM: The aim of this study is to compare the efficacy of intravitreal bevacizumab and posterior subtenons triamcinolone acetate in the management of diffuse diabetic macular edema (DME) and to evaluate their efficacy as an adjunct to modified grid laser in management of DME. DESIGN: This was a prospective, randomized clinical trial of 30 patients. MATERIALS AND METHODS: A total of 30 patients attending the medical ophthalmology clinic at a tertiary care hospital were included in the study. These 30 patients were divided into two groups. Group I (15 eyes) received intravitreal bevacizumab followed by modified grid photocoagulation 2 weeks after injection. Group II (15 eyes) received posterior subtenons triamcinolone followed by modified grid photocoagulation 2 weeks after injection. Each patient in our study was followed up at 1 week, 2 weeks, 1 month, 2 months, 3 months, and 6 months after the initial injection to record the central macular thickness (CMT) and best-corrected visual acuity (BCVA). RESULTS: Both the combination therapies have efficacy to reduce the CMT (P = 0.001). The percentage fall in CMT was greater in bevacizumab + laser group, and there was a significant difference in the CMT values at the end of the study in the bevacizumab group (P = 0.013). The mean BCVA improved in both the groups and this difference was statistically significant compared to the baseline (P = 0.005). However, there was no statistically significant difference in BCVA between the two groups at the end of the study. CONCLUSION: Both intravitreal bevacizumab and posterior subtenons triamcinolone given as an adjuvant therapy along with modified grid laser are equally efficacious in the reduction of the CMT; however, the percentage fall in the CMT was greater in bevacizumab + laser group, and there was a significant difference in the fall in CMT at all the visits as compared to a plateau in the fall of CMT in posterior subtenons triamcinolone group.

2.
Case Rep Obstet Gynecol ; 2014: 386432, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24660079

RESUMO

With the help of this case we summarize some crucial features to be picked up from history and examination before labeling a case as Bartholin's abscess or cyst. A 20-year old unmarried girl, deaf and mute since birth, was initially diagnosed to have Bartholin's abscess. On careful reexamination after inflammation subsided, a decision of excision of this tumor was taken. Intraoperatively it was found to be well encapsulated. Histopathology ascertained the diagnosis of vulval leiomyoma.

4.
Indian J Pathol Microbiol ; 54(1): 156-7, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21393904

RESUMO

Deep penetrating nevus (DPN) is a variant of melanocytic nevus which goes unrecognized due to its relative rarity and may be misinterpreted as malignant melanoma. It commonly presents in young adults as a dark pigmented lesion on the face, neck, or shoulder. A 60-year-old lady presented with a mole over the left arm of 8 years duration. A biopsy of the lesion was performed under the clinical impression of a compound nevus with suspicion of malignancy. Based on the histologic features, a diagnosis of DPN was put forward.


Assuntos
Nevo Pigmentado/diagnóstico , Nevo Pigmentado/patologia , Animais , Braço/patologia , Biópsia , Feminino , Histocitoquímica , Humanos , Microscopia , Pessoa de Meia-Idade
6.
Am J Med Genet A ; 152A(3): 759-63, 2010 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-20186788

RESUMO

We report on a 16-month-old girl with multiple swellings on her skull due to massive osteolysis, growth retardation, facial anomalies, and wrinkly skin with mosaic hypopigmentation. She also had severe hypercalcemia, which gradually returned to normal levels. The condition likely represents Gorham syndrome with systemic manifestations.


Assuntos
Anormalidades Múltiplas/genética , Deficiências do Desenvolvimento/genética , Transtornos do Crescimento/genética , Osteólise Essencial/genética , Osteólise Essencial/patologia , Crânio/patologia , Feminino , Humanos , Hipopigmentação/genética , Lactente , Anormalidades da Pele/genética , Anormalidades da Pele/patologia , Síndrome
7.
Indian J Pathol Microbiol ; 50(4): 819-21, 2007 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-18306568

RESUMO

Well differentiated villoglandular adenocarcinoma of uterine cervix is a rare tumour which usually occurs in young women. It is considered to be an indolent tumour with favorable prognosis and most of them were treated by conservative procedures. We report a 35 year old lady who came with complaints of 3 months amenorrhoea and an episode of spontaneous bleeding. Urine pregnancy test was negative. Physical examination revealed a cervical polyp. Histopathological findings were consistent with villoglandular papillary adenocarcinoma associated with high grade cervical intraepithelial neoplasia (CIN-3). Left parametrial and left ureteral involvement, proved by biopsy, causing left hydroureteronephrosis was detected. The patient was thus found to be in an advanced stage, stage- III b (FIGO). The patient is currently undergoing radiotherapy. A review of literature showed that only occasional cases showing disease spread have been reported, suggesting caution in the management and regular follow up of the patient.


Assuntos
Adenocarcinoma Papilar/complicações , Adenocarcinoma Papilar/patologia , Displasia do Colo do Útero/complicações , Displasia do Colo do Útero/patologia , Neoplasias do Colo do Útero/complicações , Neoplasias do Colo do Útero/patologia , Adenocarcinoma Papilar/diagnóstico , Adenocarcinoma Papilar/radioterapia , Anexos Uterinos/patologia , Adulto , Antineoplásicos/uso terapêutico , Cisplatino/uso terapêutico , Feminino , Humanos , Hidronefrose , Pólipos , Ureter/patologia , Neoplasias do Colo do Útero/diagnóstico , Neoplasias do Colo do Útero/radioterapia , Displasia do Colo do Útero/diagnóstico , Displasia do Colo do Útero/radioterapia
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