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Angiolipoma of testis in a case of undescended testis: A rare occurrence. 一例未降睾丸中的睾丸血管脂肪瘤：罕见病例。
IF 0.8 4区 医学
Indian Journal of Pathology and Microbiology Pub Date : 2024-04-01 Epub Date: 2023-07-26 DOI: 10.4103/ijpm.ijpm_968_22
Sudha Sharma, Puneet Jain
{"title":"Angiolipoma of testis in a case of undescended testis: A rare occurrence.","authors":"Sudha Sharma, Puneet Jain","doi":"10.4103/ijpm.ijpm_968_22","DOIUrl":"10.4103/ijpm.ijpm_968_22","url":null,"abstract":"","PeriodicalId":13488,"journal":{"name":"Indian Journal of Pathology and Microbiology","volume":null,"pages":null},"PeriodicalIF":0.8,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70763828","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Fungal infections in the era of COVID-19: Time to awaken to the Titanic. COVID-19时代的真菌感染：唤醒 "泰坦尼克号 "的时候到了。
IF 0.8 4区 医学
Indian Journal of Pathology and Microbiology Pub Date : 2024-04-01 Epub Date: 2023-07-26 DOI: 10.4103/ijpm.ijpm_859_22
Nidhi Singla, Yashik Bansal
{"title":"Fungal infections in the era of COVID-19: Time to awaken to the Titanic.","authors":"Nidhi Singla, Yashik Bansal","doi":"10.4103/ijpm.ijpm_859_22","DOIUrl":"10.4103/ijpm.ijpm_859_22","url":null,"abstract":"","PeriodicalId":13488,"journal":{"name":"Indian Journal of Pathology and Microbiology","volume":null,"pages":null},"PeriodicalIF":0.8,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70763018","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Disseminated multiloculated peritoneal inclusion cysts: Bubble trouble in belly 弥散性多灶性腹膜包涵囊肿肚子里的泡沫麻烦
IF 1 4区 医学
Indian Journal of Pathology and Microbiology Pub Date : 2024-02-19 DOI: 10.4103/ijpm.ijpm_556_23
M. Osama, Aditi Aggarwal, Seema Rao, Amitabh Yadav, Ritu Verma
{"title":"Disseminated multiloculated peritoneal inclusion cysts: Bubble trouble in belly","authors":"M. Osama, Aditi Aggarwal, Seema Rao, Amitabh Yadav, Ritu Verma","doi":"10.4103/ijpm.ijpm_556_23","DOIUrl":"https://doi.org/10.4103/ijpm.ijpm_556_23","url":null,"abstract":"\u0000 Multiloculated peritoneal inclusion cysts, usually arise from peritoneal mesothelium lining the serous cavity of the abdomen, pelvis and retroperitoneum. These lesions can be incidentally found on imaging or during surgery, and confirmation of the diagnosis is done by radiological imaging, histomorphology and immunohistochemical findings. Although fewer than 200 cases of solitary peritoneal inclusion cysts have been reported, their occurrence in a disseminated fashion has hardly ever been described in literature. Herein, we report a case of multiloculated peritoneal inclusion cysts that involved the whole abdominal and pelvic cavity and were successfully treated with surgery.","PeriodicalId":13488,"journal":{"name":"Indian Journal of Pathology and Microbiology","volume":null,"pages":null},"PeriodicalIF":1.0,"publicationDate":"2024-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139958876","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A serious warning: A case report on localized amyloidosis of the oral cavity 严重警告口腔局部淀粉样变性病例报告
IF 1 4区 医学
Indian Journal of Pathology and Microbiology Pub Date : 2024-02-19 DOI: 10.4103/ijpm.ijpm_720_23
Sharon John, Priyambadha Subba, Aravindhan Aramugam, Shalini Gupta, Richa Khanna
{"title":"A serious warning: A case report on localized amyloidosis of the oral cavity","authors":"Sharon John, Priyambadha Subba, Aravindhan Aramugam, Shalini Gupta, Richa Khanna","doi":"10.4103/ijpm.ijpm_720_23","DOIUrl":"https://doi.org/10.4103/ijpm.ijpm_720_23","url":null,"abstract":"\u0000 Amyloidosis is a relatively rare condition with an array of complex pathophysiology. Localized amyloidosis is a rare and benign condition that practically never results in any clinical repercussions in the head and neck area. Multiple soft nodules of the tongue, lip, and cheek are the most commonly described defining characteristics of localized oral amyloidosis. These nodules originate due to the proliferation of abnormally folded protein aggregates in the body’s extracellular tissue compartments, which destroy organ structure and function. Herein, we address the case of a female infant aged one with a smooth nodule in the labial mucosa who was diagnosed with primary localized amyloidosis. When a patient is diagnosed with amyloidosis of the oral mucosa, the possibility of systemic amyloidosis or an underlying plasma cell dyscrasia must be ruled out. Surgical treatment may be beneficial for eliminating any functional impairment if primary localized amyloidosis is established.","PeriodicalId":13488,"journal":{"name":"Indian Journal of Pathology and Microbiology","volume":null,"pages":null},"PeriodicalIF":1.0,"publicationDate":"2024-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139958592","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Neuroendocrine differentiation in a metachronous metastatic deposit in a case of mature growing ovarian teratoma: A rare occurrence 一例生长成熟的卵巢畸胎瘤转移性沉积物中的神经内分泌分化：罕见病例
IF 1 4区 医学
Indian Journal of Pathology and Microbiology Pub Date : 2024-02-01 DOI: 10.4103/ijpm.ijpm_339_23
Divakar Jain, S. Patkar, Jasmine Agarwal, Santosh Menon, M. Goel
{"title":"Neuroendocrine differentiation in a metachronous metastatic deposit in a case of mature growing ovarian teratoma: A rare occurrence","authors":"Divakar Jain, S. Patkar, Jasmine Agarwal, Santosh Menon, M. Goel","doi":"10.4103/ijpm.ijpm_339_23","DOIUrl":"https://doi.org/10.4103/ijpm.ijpm_339_23","url":null,"abstract":"\u0000 Growing teratoma syndrome is a rare condition seen in non seminomatous germ cell tumor after completion of chemotherapy. Ectodermal, mesodermal and endodermal differentiation is commonly seen in mature teratoma. neuroendocrine differentiation in a metastatic deposit of mature teratoma is rarely reported. We are presenting a case of neuroendocrine differentiation in a long standing metastatic deposit of a mature teratoma.","PeriodicalId":13488,"journal":{"name":"Indian Journal of Pathology and Microbiology","volume":null,"pages":null},"PeriodicalIF":1.0,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139684860","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cytomorphological traits of fine-needle aspirates of hyalinizing trabecular tumor of the thyroid gland: A brief report. 甲状腺透明小梁瘤细针穿刺细胞形态学特征：简要报告。
IF 1 4区 医学
Indian Journal of Pathology and Microbiology Pub Date : 2024-01-01 DOI: 10.4103/ijpm.ijpm_405_22
Fei Wang, Yufei Liu
{"title":"Cytomorphological traits of fine-needle aspirates of hyalinizing trabecular tumor of the thyroid gland: A brief report.","authors":"Fei Wang, Yufei Liu","doi":"10.4103/ijpm.ijpm_405_22","DOIUrl":"10.4103/ijpm.ijpm_405_22","url":null,"abstract":"<p><strong>Background: </strong>The incidence of thyroid tumor is increasing, and preoperative diagnosis of hyalinizing trabecular tumor (HTT) is difficult.</p><p><strong>Aim: </strong>To investigate the cytological features of HTT of the thyroid gland.</p><p><strong>Settings and design: </strong>A retrospective observational study.</p><p><strong>Materials and methods: </strong>Ultrasonography, preoperative needle aspiration cytology, postoperative histopathology, immunohistochemistry, and BRAF V600E gene test were performed in five patients with HTT to analyze the pathological characteristics of the patients and review the relevant literature.</p><p><strong>Results: </strong>Four female and one male patients with HTT were recruited. Fine-needle aspiration cytology (FNAC) showed bloodstained background tumor cells with multiple morphologies. The tumor cells exhibited ovoid nuclei, abundant cytoplasm, fine chromatin, nuclear crowding and overlapping, and small nucleoli. Focal nuclear pseudoinclusions and grooves were present. No papillary structures or psammoma bodies were observed. In all cases, tumor cells were radially distributed around the eosinophilic extracellular matrix. In 40% (2 in 5) of cases, trabecular patterns of elongated tumor cells were present, with their nuclei staggered along the longitudinal axis of tumor cells in the trabeculae. FNAC suggested two cases of HTT and three cases of papillary thyroid cancer. Post-operational biopsy indicated they were HTT cases.</p><p><strong>Conclusion: </strong>HTT is a rare thyroid tumor with non-specific clinical manifestations. It can be misinterpreted as papillary thyroid carcinoma by FNAC. However, its cytomorphological traits are helpful in the diagnosis. In combination with FNAC, immunohistochemistry, and molecular testing, HTT can be accurately diagnosed.</p>","PeriodicalId":13488,"journal":{"name":"Indian Journal of Pathology and Microbiology","volume":null,"pages":null},"PeriodicalIF":1.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70762852","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Neurosarcoidosis: Frozen section rescue for a big mimicker - A case report. 神经肉瘤病：冷冻切片抢救大模仿者--病例报告。
IF 1 4区 医学
Indian Journal of Pathology and Microbiology Pub Date : 2024-01-01 DOI: 10.4103/ijpm.ijpm_638_22
Farhan A Siddiqui, Jawad Al-Khalaf, Yusef Al-Marzooq, Jaffer Al-Obaid, Abdulhakim Y M Almarzooq
{"title":"Neurosarcoidosis: Frozen section rescue for a big mimicker - A case report.","authors":"Farhan A Siddiqui, Jawad Al-Khalaf, Yusef Al-Marzooq, Jaffer Al-Obaid, Abdulhakim Y M Almarzooq","doi":"10.4103/ijpm.ijpm_638_22","DOIUrl":"10.4103/ijpm.ijpm_638_22","url":null,"abstract":"<p><p>Neurosarcoidosis is an uncommon but potentially serious manifestation of sarcoidosis. Diagnosis may be particularly challenging especially when neurosarcoidosis occurs in isolation or is the initial presentation of the systemic disease. The authors take this opportunity to report a case of neurosarcoidosis, presenting as the first manifestation of the disease, diagnosed on frozen section, occurring in a 43-year-old male patient with no past history or manifestation of sarcoidosis.</p>","PeriodicalId":13488,"journal":{"name":"Indian Journal of Pathology and Microbiology","volume":null,"pages":null},"PeriodicalIF":1.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70762984","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
To interpret and analyze the changing patterns of histology and direct immunofluorescence findings in membranoproliferative glomerulonephritis. 解读和分析膜增生性肾小球肾炎组织学和直接免疫荧光结果的变化规律。
IF 1 4区 医学
Indian Journal of Pathology and Microbiology Pub Date : 2024-01-01 DOI: 10.4103/ijpm.ijpm_1015_22
Pragnya P Nayak, Pranati Pradhan, Dilleswari Pradhan, Nachiketa Mohapatra, Sarojini Raman, Pranabandhu Sahoo
{"title":"To interpret and analyze the changing patterns of histology and direct immunofluorescence findings in membranoproliferative glomerulonephritis.","authors":"Pragnya P Nayak, Pranati Pradhan, Dilleswari Pradhan, Nachiketa Mohapatra, Sarojini Raman, Pranabandhu Sahoo","doi":"10.4103/ijpm.ijpm_1015_22","DOIUrl":"10.4103/ijpm.ijpm_1015_22","url":null,"abstract":"<p><strong>Background: </strong>Membranoproliferative glomerulonephritis has in the recent past been regrouped into immune complex-mediated (ICM MPGN) disease (driven by the classical complement pathway) and complement-mediated (C3GN) disease (driven by the alternative complement pathway) based on pathogenetic role of alternative complement pathway and immunofluorescence deposits. The proposed regrouping lent therapeutic and prognostic support in managing the disease of MPGN.</p><p><strong>Aims and objectives: </strong>The present study is undertaken to study the patterns of MPGN based on histopathological and DIF examination and sub-categorize the cases into mainly complement dominant and immune complex-mediated diseases for better prognostic and therapeutic utility.</p><p><strong>Materials and methods: </strong>This is a prospective observational study carried out in a tertiary care center over a period of 2 yrs. The clinically suspected cases of MPGN were subjected to histopathologic and direct immunofluorescence examination (DIF), and the findings were interpreted in light of complement-mediated and immune complex-mediated MPGN.</p><p><strong>Results: </strong>Out of 620 renal biopsies, diagnosis of MPGN was confirmed both on histopathology and DIF in 36 cases accounting for 5.8% of all biopsies. Based on DIF findings, the various groups comprised 20 cases (55.6%) of immune complex deposits, 11 (30.5%) of C3 dominant picture, and 5 (13.9%) of Nil immune deposits. On analysis of the patterns on DIF, 16 cases (80%) of C3 + Ig group and 6 (54.5%) of C3GN group showed predominantly MPGN pattern. Crescentic glomerulonephritis, global glomerulosclerosis, and interstitial fibrosis were markedly observed in C3GN group.</p><p><strong>Conclusion: </strong>DIF is of immense prognostic and therapeutic value in managing cases of MPGN.</p>","PeriodicalId":13488,"journal":{"name":"Indian Journal of Pathology and Microbiology","volume":null,"pages":null},"PeriodicalIF":1.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70761242","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Isolated bone marrow candidiasis in an immunocompetent elderly. 一名免疫力低下的老人患上了孤立的骨髓念珠菌病。
IF 1 4区 医学
Indian Journal of Pathology and Microbiology Pub Date : 2024-01-01 DOI: 10.4103/ijpm.ijpm_918_21
Deval B Dubey, Mili Jain, Shailendra P Verma, Preeti Agarwal
{"title":"Isolated bone marrow candidiasis in an immunocompetent elderly.","authors":"Deval B Dubey, Mili Jain, Shailendra P Verma, Preeti Agarwal","doi":"10.4103/ijpm.ijpm_918_21","DOIUrl":"10.4103/ijpm.ijpm_918_21","url":null,"abstract":"","PeriodicalId":13488,"journal":{"name":"Indian Journal of Pathology and Microbiology","volume":null,"pages":null},"PeriodicalIF":1.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70763583","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Adenomyoepithelial adenosis mimicking phylloides: A diagnostic dilemma. 腺肌瘤上皮腺病模仿蝶形花：诊断难题。
IF 1 4区 医学
Indian Journal of Pathology and Microbiology Pub Date : 2024-01-01 DOI: 10.4103/ijpm.ijpm_925_22
Jyoty Singh, Atin Singhai, Suresh Babu, Kulranjan Singh, Anand Mishra
{"title":"Adenomyoepithelial adenosis mimicking phylloides: A diagnostic dilemma.","authors":"Jyoty Singh, Atin Singhai, Suresh Babu, Kulranjan Singh, Anand Mishra","doi":"10.4103/ijpm.ijpm_925_22","DOIUrl":"10.4103/ijpm.ijpm_925_22","url":null,"abstract":"<p><p>Benign proliferative breast diseases are well recognized in young females. Benign biphasic proliferation of epithelial and myoepithelial cells has been observed, among which adeno-myoepithelial adenosis is one of the rare morphologies published in the literature with the tendency to recur and poses a risk for low-grade malignant transformation. Here, we report a case of a young female who had a history of recurrent breast lump mimicking phyllodes tumor and eventually diagnosed as adeno-myoepithelial adenosis on histopathological examination. Benign proliferative breast diseases are well recognized in young females. Benign biphasic proliferation of epithelial and myoepithelial cells has been observed, among which adeno-myoepithelial adenosis is one of the rare morphologies published in the literature with the tendency to recur and poses a risk for low-grade malignant transformation. Here, we report a case of a young female who had a history of recurrent breast lump mimicking phyllodes tumor and eventually diagnosed as adeno-myoepithelial adenosis on histopathological examination.</p>","PeriodicalId":13488,"journal":{"name":"Indian Journal of Pathology and Microbiology","volume":null,"pages":null},"PeriodicalIF":1.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70763662","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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