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Dive into the research topics where Surbhi Goyal is active.

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Featured researches published by Surbhi Goyal.


Journal of Obstetrics and Gynaecology Research | 2014

Acquired uterine arteriovenous malformation developing in retained products of conception: A diagnostic dilemma

Surbhi Goyal; Ankur Goyal; Surbhi Mahajan; Shikha Sharma; Geeta Dev

Abnormal uterine bleeding in the postabortal period requires meticulous diagnostic work‐up to decide proper management. Imaging modalities including Doppler sonography and magnetic resonance imaging in concert with clinical and laboratory findings are useful to narrow the differential diagnoses but are not definitive. Presence of increased uterine vascularity and arteriovenous shunting is non‐specific and can be detected in a variety of conditions including retained trophoblastic tissue, gestational trophoblastic disease, arteriovenous malformation (AVM), placental polyp and vascular neoplasm. We present here a case of a multiparous woman with unexplained postabortal bleeding posing a diagnostic challenge. Excluding the possibility of AVM before attempting dilatation and curettage in such a clinical scenario is crucial to prevent catastrophic bleeding.


Journal of Obstetrics and Gynaecology Research | 2014

Endodermal sinus tumor of vagina posing a diagnostic challenge and managed by chemotherapy and novel posterior sagittal surgical approach: Lessons learned

Surbhi Goyal; Archana Puri; Kiran Mishra; Satish Kumar Aggarwal; Manisha Kumar; Pitamber Sonaker

Vaginal germ cell tumor (GCT) is a rare gynecological malignancy with no more than 100 reported cases in the international medical literature. It is an unusual, but an important, cause of premenarchal vaginal bleeding in a child. This article describes a 2‐year‐old child with vaginal GCT, initially misdiagnosed as rhabdomyosarcoma (on imprint smear cytology) and then as clear cell adenocarcinoma. The authors highlight the salient differentiating clinical, radiological and histological features to prevent misdiagnosis in future. The report emphasizes the need for increased awareness and screening for vaginal GCT by estimation of serum α‐fetoprotein levels, in all patients with premenarchal vaginal bleeds, to prevent inadvertent operative interventions.


Indian Journal of Medical Research | 2016

Diagnostic utility of Wilms' tumour-1 protein (WT-1) immunostaining in paediatric renal tumours

Surbhi Goyal; Kiran Mishra; Urvee Sarkar; Satendra Sharma; Anita Kumari

Background & objectives: Renal tumours constitute about 7 per cent of all neoplasms in children. It is important to differentiate Wilms’ tumour (commonest tumour) from non-Wilms’ tumours. The aim of this study was to evaluate the immunoexpression and diagnostic role of Wilms’ tumour-1 protein (WT1) in paediatric renal tumours. Methods: A total of 53 cases of renal tumours in children (below 18 yr) who underwent total nephrectomy were included in this retrospective study. WT1 immunostaining was done using mouse monoclonal WT1 antibody (clone: 6F-H2). Results: Of the 53 cases, 38 (72%) were of Wilms’ tumour. Non-Wilms’ group (15) included six cases of mesoblastic nephroma (MN), two each of clear cell sarcoma (CCSK), renal cell carcinoma (RCC) and peripheral neuroectodermal tumour (PNET) and one each of angiomyolipoma (AML), rhabdomyosarcoma (RMS) and malignant rhabdoid tumour (MRT). Proportion of WT1 positivity in Wilms’ tumour was 100 per cent in contrast to 26.7 per cent in non-Wilms’ tumours (P<0.001). Epithelial and blastemal components of Wilms’ tumour showed moderate (2+) nuclear and cytoplasmic staining in 80 (24/30) and 75 per cent (24/32) cases, respectively. MN, PNET, CCSK and AML were negative for WT1. RMS, RCC and MRT showed cytoplasmic staining, strongest in RMS. No significant association was seen between WT1 expression and NWTSG (National Wilms’ Tumor Study Group) stage. Interpretation & conclusions: WT1 helps to differentiate Wilms’ tumour from other paediatric renal tumours. It may help in differentiating the two subgroups of Wilms’ tumour which have distinct molecular pathogenesis and biological behaviour, however, further prospective studies are required for validation of this hypothesis.


Medicina Oral Patologia Oral Y Cirugia Bucal | 2015

Role of FNAC in the diagnosis of intraosseous jaw lesions.

Surbhi Goyal; Sonal Sharma; Mrinalini Kotru; Neelima Gupta

Background FNAC of intraosseous jaw lesions has not been widely utilized for diagnosis due to rarity and diversity of these lesions, limited experience and lack of well established cytological features. Aim of the study was to determine the role of FNAC in the diagnosis of intraosseous jaw swellings. Material and Methods 42 patients underwent FNAC over a period of 7 years (2007-2013), of which 37 (88.1%) aspirates were diagnostic. Histopathology correlation was available in 33 cases and diagnostic accuracy of FNAC was calculated. Results Lesions were categorized into inflammatory 3, cysts/hamartomas 15 and neoplasms 19. Mandibular and maxillary involvement was seen in 21 and 16 patients respectively. Of these, benign cysts and malignant lesions were commonest, accounting for 27% lesions (10 cases) each. One case of cystic ameloblastoma was misdiagnosed as odontogenic cyst on cytology. Overall, sensitivity and specificity of FNAC were 94.7% and 100% respectively with a diagnostic accuracy of 97.3%. Definitive categorization of giant cell lesions, fibro-osseous lesions, odontogenic tumors and cystic lesions was not feasible on FNAC. Conclusions FNAC is a simple, safe and minimally invasive first line investigation which can render an accurate preoperative diagnosis of intraosseous jaw lesions, especially the malignant ones in the light of clinic-radiological correlation. Key words: Jaw swellings, intraosseous, FNAC.


Journal of Obstetrics and Gynaecology | 2015

Ovarian lymphangioma masquerading as ectopic pregnancy: A clinical dilemma

Surbhi Goyal; Sonal Sharma; Mrinalini Kotru; A. Sharma

Fujisawa T, Watanabe J, Kamata Y et al. 2003. Effect of p53 gene transfection on vascular endothelial growth factor expression in endometrial cancer cells. Experimental and Molecular Pathology 74:276–281. Hui P, Kelly M, O’Malley DM et al. 2005. Minimal uterine serous carcinoma: a clinicopathological study of 40 cases. Modern Pathology 18:75–82. Lee SC, Kaunitz AM, Sanchez-Ramos L et al. 2010. The oncogenic potential of endometrial polyps: a systematic review and meta-analysis. Obstetrics and Gynecology 116:1197–1205. Lockwood CJ. 2011. Mechanisms of normal and abnormal endometrial bleeding. Menopause 18:408–411. Pathiraja P, Dhar S, Haldar K. 2013. Serous endometrial intraepithelial carcinoma: a case series and literature review. Cancer Management and Research 5:117–122. Sherman ME. 2000. Theories of endometrial carcinogenesis: a multidisciplinary approach. Modern Pathology 13:295–308. Soslow RA, Pirog E, Isacson C. 2000. Endometrial intraepithelial carcinoma with associated peritoneal carcinomatosis. American Journal of Surgical Pathology 24:726–732. Stewart EA, Nowak RA. 1996. Leiomyoma-related bleeding: a classic hypothesis updated for the molecular era. Human Reproduction Update 2:295–306. Trahan S, Tetu B, Raymond P. 2005. Serous papillary carcinoma of the endometrium arising from endometrial polyps: a clinical, histological, and immunohistochemical study of 13 cases. Human Pathology 36: 1316–1321.


Diagnostic Cytopathology | 2015

Diagnostic role and limitations of FNAC in oral and jaw swellings.

Surbhi Goyal; Sonal Sharma; Preeti Diwaker

Fine‐needle aspiration cytology (FNAC) of oral lesions has not been widely utilized for diagnosis due to rarity and diversity of lesions, peculiar anatomy of maxillofacial region, difficulty in aspirating these lesions, and limited experience. Aim of this study was to determine the role of FNAC in the diagnosis of oral and jaw swellings.


American Journal of Dermatopathology | 2015

Neurocristic Hamartoma With Lymph Node Involvement: A Diagnostic Dilemma.

Surbhi Goyal; Vinod Kumar Arora; Lipy Gupta; Archana Singal; Navneet Kaur

Neurocristic hamartoma (NH) is a rare dermal melanocytic lesion that is formed due to the aberrant development of neural crest-derived melanocytes during their course of migration through the dermis at the time of embryogenesis. Here, we describe a case of NH in a 6-year-old boy who clinically presented with diffuse plaque-type blue nevus on his scalp with a contiguous extension into the cervical region and lymph node involvement. A subcutaneous nodule displaying a marked histological heterogeneity with lymph node involvement is a very unusual and diagnostically challenging presentation of NH. The importance of an accurate diagnosis of NH lies in the fact that malignant transformation can rarely occur within these lesions over an unpredictable time course and remain undetected, rendering clinical management difficult. Although our child had a benign course after a follow-up of 5 years despite lymph node involvement, the possible risk of development of malignant melanoma in such a lesion warrants long-term surveillance. This case report highlights the unusual clinical presentation and histopathological features of this rare entity along with a relevant review of the literature. The present case also underscores the concept that sentinel lymph node involvement in certain melanocytic lesions in children must not be mistaken for malignant melanoma.


Diagnostic Cytopathology | 2014

Role of FNAC in palpable chest wall lesions in developing country

Surbhi Goyal; Sonal Sharma; Nidhi Bahl

Palpable chest wall lesions are unusual manifestation of an underlying thoracic pathology and it is difficult to diagnose them with their diverse spectrum ranging from benign to malignant. Considering the exposure of patient to invasive biopsy/excision and the risk of local complications, FNAC is now being increasingly used in the primary assessment of these lesions. Objectives of this study were to report the spectrum of chest wall lesions in the population of a developing country and evaluating the diagnostic role of FNAC.


Journal of Cytology | 2017

Intestinal GIST masquerading as an ovarian mass: Diagnosed on FNAC

Surbhi Goyal; Vinod Kumar Arora; Mohit Kumar Joshi; Navjeevan Singh; Gita Radhakrishnan

The preoperative diagnosis of metastatic intestinal gastrointestinal stromal tumors (GIST) on cytology can be quite difficult at times. The present case characterizes the cytomorphological and immunocytochemical features of GIST, emphasizing the utility of fine-needle aspiration cytology (FNAC) in the evaluation of spindle cell tumors of gastrointestinal tract. An accurate and early diagnosis of GIST affects the treatment, primarily allowing the use of tyrosine kinase inhibitors in unresectable or metastatic cases. Presence of highly cellular fragments of spindle-to-oval cells with variable degree of pleomorphism, atypia, and necrosis supplemented by immunocytochemistry can render a cytological diagnosis of GIST in dilemmatic clinical situations. Our case highlights the diagnostic role of FNAC in the evaluation of a pelvic mass, which was clinicoradiologically misdiagnosed as ovarian carcinoma.


Journal of Cytology | 2017

Cutaneous basal cell carcinoma with mixed histology: Cytomorphological features of two unusual cases

Surbhi Goyal; Ruchi Rathore; Sonal Sharma; Vinod Kumar Arora; Gopal K Das; Archana Singal

Cutaneous basal cell carcinoma (BCC) is a slow growing locally aggressive malignant tumor. It is usually diagnosed on histopathological examination of the excised biopsy. Recently, fine needle aspiration cytology (FNAC) is emerging as a simple alternative technique for rapid diagnostic work of nodular and plaque-like skin lesions. We report the cytomorphological features of two cases of cutaneous BCC having unusual clinical presentation and mixed histology (MH); emphasizing the diagnostic difficulties encountered on cytology, the plausible explanation and the precautions to keep in mind to avoid misdiagnosis.

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Sonal Sharma

University College of Medical Sciences

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Ankur Goyal

All India Institute of Medical Sciences

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Mrinalini Kotru

University College of Medical Sciences

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Vinod Kumar Arora

University College of Medical Sciences

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Archana Singal

University College of Medical Sciences

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Geeta Dev

University College of Medical Sciences

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Kiran Mishra

University College of Medical Sciences

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Navneet Kaur

University College of Medical Sciences

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Preeti Sharma

Central Drug Research Institute

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