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1.
J Cytol ; 41(2): 105-109, 2024.
Article in English | MEDLINE | ID: mdl-38779602

ABSTRACT

Background: Atypical glandular cells (AGCs) diagnosis on Pap (Papanicolaou) smears are uncommon and may represent various benign and malignant lesions. Objective: This study aims to report the incidence of AGC on Pap smear, to study the relationship of AGC with malignancy, and to determine cytomorphological features that help in predicting malignancy. Materials and Methods: Retrospective analytical study conducted in the Department of Oncopathology at Tertiary Cancer and Research Institute. In this retrospective study, we included cases diagnosed with AGC between July 2017 to July 2022. All slides were reviewed and subclassified according to the Bethesda 2014 classification system (TBS). The predetermined cytomorphological features observed in the smears were recorded. The follow-up histopathological diagnoses of the cases were retrieved. The significant cytomorphological and clinicopathological findings for malignancy were determined. Results: Pearson χ2 test with SPSS software version 22 to compare cytologic features of cases with benign and malignant follow-up. The significant cytomorphological features observed in neoplastic cases were cells in 3-dimensional clusters, nuclear overlapping, reniform nucleus, irregular nuclear membrane, increased nuclear size, single macronucleoli, engulfed neutrophils, and prominently vacuolated cytoplasm. Conclusions: The diagnosis of AGC on cytology is associated with clinically significant lesions, and cytomorphologic parameters can be used to predict the benign and malignant outcome.

2.
Eur Arch Otorhinolaryngol ; 281(3): 1571-1579, 2024 Mar.
Article in English | MEDLINE | ID: mdl-38010402

ABSTRACT

INTRODUCTION: Medullary carcinoma (MTC) is a rare neuroendocrine thyroid neoplasm. The international medullary thyroid carcinoma grading scheme (IMTCGS), which has prognostic significance, has been introduced recently. The present study graded MTC cases using the IMTCGS and evaluated it in our study cohort. METHODS: All MTC thyroidectomy cases over 6 years were evaluated. Low-grade (LG) and high-grade (HG) were compared. Survival analysis included overall survival (OS), loco-regional free survival and distant metastasis free survival (DMFS). RESULTS: Of 32 cases, 31.25% were HG and 68.75% LG. The mean age was 44.0 years and M:F ratio 1:1.146. HG patients were older and had tumour cells with high-grade nuclear features and prominent nucleoli and showed distant metastasis. Necrosis was found more in patients with high grade nuclear features. There was discordance between the high Ki67 (60%) and increased mitotic activity (20%). Univariate survival analysis revealed poor DMFRS and OS in the cohorts with high grade, Ki67 > 5% and coagulative necrosis. The multivariate cox regression analysis showed IMTCGS significantly associated with overall survival (HR 28.30, p = 0.009) and DMFS (HR 15.70, p = 0.02). DISCUSSION AND CONCLUSION: This is the first Indian study evaluating IMTCGS, a very simple and convenient grading system that can be readily used in any tertiary health care centre. IHC for Ki 67 should mandatorily be done irrespective of the low mitotic activity on the HPE and necrosis should be diligently searched in cases with high-grade nuclear morphology. HG MTC cohorts were associated with poor OS as well as DMFRS.


Subject(s)
Carcinoma, Neuroendocrine , Thyroid Neoplasms , Humans , Adult , Ki-67 Antigen , Tertiary Care Centers , Carcinoma, Neuroendocrine/surgery , Carcinoma, Neuroendocrine/pathology , Prognosis , Thyroid Neoplasms/pathology , Necrosis , Retrospective Studies
3.
Diagn Cytopathol ; 49(1): 127-131, 2021 Jan.
Article in English | MEDLINE | ID: mdl-32910561

ABSTRACT

OBJECTIVE: To determine the role of routine cervical Pap smears in detecting endometrial carcinomas. METHOD: A retrospective study was carried out from the histopathology archives for cases diagnosed as endometrial carcinomas with Pap smears within 6 months before histological diagnosis. The demographic details, reports of Pap smears and other tumor parameters on histopathology were noted. RESULTS: We identified 380 of 482 cases of endometrial carcinoma with a documented Pap smear within 6 months before histopathogical diagnosis. Out of 380 cases, 187 cases (49.2%) had shown abnormalities on Pap smear of which 80 cases (42%) were diagnosed as atypical glandular cells and 78 cases (41.7%) were diagnosed as adenocarcinoma. The presence of glandular abnormality on Pap smear significantly correlated with the tumor type, myometrial invasion and cervical involvement on histopathology (P < .05). Cases which had higher FIGO staging also had a higher detection rate on Pap smear (P < .05). CONCLUSION: The Pap smear may help in detection of endometrial carcinoma especially in cases with type 2 endometrial carinomas, tumor with cervical involvement and/or advanced FIGO stage.


Subject(s)
Cervix Uteri/pathology , Endometrial Neoplasms/diagnosis , Endometrial Neoplasms/pathology , Adenocarcinoma/diagnosis , Adenocarcinoma/pathology , Female , Humans , Middle Aged , Papanicolaou Test/methods , Retrospective Studies , Uterine Cervical Neoplasms/diagnosis , Uterine Cervical Neoplasms/pathology , Vaginal Smears/methods
4.
Urology ; 116: e7-e8, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29567016

ABSTRACT

Primary renal synovial sarcoma (PRSS) is a rare entity. It should be considered as one of the differential diagnoses of spindle cell tumors of the kidney. Immunohistochemistry and genetic translocation studies should be used to confirm the diagnosis. Because of a lack of consistent literature data regarding the treatment options, management of PRSS remains a therapeutic challenge. In view of the chemosensitive nature of the tumor, we propose a multimodality treatment in form of surgery and chemotherapy in patients with PRSS. Here we report a rare case of PRSS in a 17-year-old adolescent.


Subject(s)
Kidney Neoplasms/diagnostic imaging , Sarcoma, Synovial/diagnostic imaging , Tomography, X-Ray Computed , Adolescent , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Biomarkers, Tumor/analysis , Combined Modality Therapy , Doxorubicin/administration & dosage , Humans , Ifosfamide/administration & dosage , Kidney Neoplasms/chemistry , Kidney Neoplasms/pathology , Kidney Neoplasms/therapy , Neoadjuvant Therapy , Nephrectomy , Sarcoma, Synovial/chemistry , Sarcoma, Synovial/pathology , Sarcoma, Synovial/therapy
5.
Indian J Pathol Microbiol ; 58(2): 223-5, 2015.
Article in English | MEDLINE | ID: mdl-25885140

ABSTRACT

Occurrence of carcinoid tumors in the esophagus is exceedingly rare. We present a case of an atypical carcinoid in the mid esophagus in a 56-year-old male, presenting with dysphagia. Esophagectomy was performed followed by postoperative chemotherapy. Histopathological and immunohistochemical studies were carried out. The patient succumbed to liver and lung metastasis, 6 months after the initial diagnosis, highlighting the poor prognosis of the condition.


Subject(s)
Carcinoid Tumor/diagnosis , Carcinoid Tumor/pathology , Esophageal Neoplasms/diagnosis , Esophageal Neoplasms/pathology , Esophagus/pathology , Biomarkers, Tumor/analysis , Carcinoid Tumor/drug therapy , Carcinoid Tumor/surgery , Chromogranin A/analysis , Drug Therapy , Esophageal Neoplasms/drug therapy , Esophageal Neoplasms/surgery , Esophagectomy , Esophagus/surgery , Histocytochemistry , Humans , Immunohistochemistry , Ki-67 Antigen/analysis , Male , Microscopy , Middle Aged
6.
Indian J Pathol Microbiol ; 57(2): 305-7, 2014.
Article in English | MEDLINE | ID: mdl-24943773

ABSTRACT

Ameloblastoma is a neoplasm of odontogenic epithelium, especially of enamel organ-type tissue that has not undergone differentiation to the point of hard tissue formation. Granular cell ameloblastoma is a rare condition, accounting for 3-5% of all ameloblastoma cases. A 30-year-old female patient presented with the chief complaint of swelling at the right lower jaw region since 1 year. Orthopantomogram and computed tomography scan was suggestive of primary bone tumor. Histopathologically, diagnosis of granular cell ameloblastoma of right mandible was made.


Subject(s)
Ameloblastoma/diagnosis , Ameloblastoma/pathology , Mandible/pathology , Mandibular Neoplasms/diagnosis , Mandibular Neoplasms/pathology , Adult , Ameloblastoma/surgery , Female , Histocytochemistry , Humans , Mandible/diagnostic imaging , Mandibular Neoplasms/surgery , Microscopy , Tomography, X-Ray Computed
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