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Journals Indian Journal of Pathology & ...

Indian Journal of Pathology & Microbiology

https://read.qxmd.com/read/37530374/catechism-quiz-20
#1
JOURNAL ARTICLE
Bharat Rekhi
No abstract text is available yet for this article.
2023: Indian Journal of Pathology & Microbiology
https://read.qxmd.com/read/37530373/a-rare-cause-of-anti-nucleolar-th-to-antibody-seropositivity-in-interstitial-pneumonia-with-autoimmune-features-undifferentiated-connective-tissue-disease
#2
LETTER
Chhabra Seema, Dhir Varun, Dhooria Sahajal, Walker R Minz
No abstract text is available yet for this article.
2023: Indian Journal of Pathology & Microbiology
https://read.qxmd.com/read/37530372/aggressive-large-b-cell-lymphoma-mimicking-turban-tumor
#3
LETTER
Ashish Singh, Charanpreet Singh, Ridhi Sood, Gaurav Prakash
No abstract text is available yet for this article.
2023: Indian Journal of Pathology & Microbiology
https://read.qxmd.com/read/37530371/atypical-clinical-presentation-of-zika-virus-from-india
#4
LETTER
Suruchi Shukla, Pragya D Yadav, Sunita Patil, Amita Jain, Vikasendu Aggarawal
No abstract text is available yet for this article.
2023: Indian Journal of Pathology & Microbiology
https://read.qxmd.com/read/37530370/covid-19-reactivating-cmv-or-cmv-complicating-covid-19-a-need-to-conquer
#5
LETTER
Areena Hoda Siddiqui, Anju Shukla, Dayaram Yadav
No abstract text is available yet for this article.
2023: Indian Journal of Pathology & Microbiology
https://read.qxmd.com/read/37530369/reporting-an-immune-mediated-neonatal-hyperbilirubinemia-following-rh-d-isoimmunization-in-an-indian-term-newborn-bearing-a-mfa-b-rh-d-positive-phenotype
#6
LETTER
Manish Raturi, Bhawana Adhikari, Aastha Kalra, Mansi Kala, Anuradha Kusum
No abstract text is available yet for this article.
2023: Indian Journal of Pathology & Microbiology
https://read.qxmd.com/read/37530368/teratoid-wilm-s-tumor-with-cryptorchidism
#7
JOURNAL ARTICLE
Nishav Garg, Pavneet K Selhi, Ankita Soni
No abstract text is available yet for this article.
2023: Indian Journal of Pathology & Microbiology
https://read.qxmd.com/read/37530367/leiomyoma-of-the-palatine-tonsil-report-of-a-rare-and-unusual-tumor-at-this-site
#8
JOURNAL ARTICLE
Andleeb Abrari, Aarti Tyagi, Urmi Mukherjee
A leiomyoma is a remarkably rare cause of a benign, one-side tonsillar enlargement. The diagnosis is essentially histologic and will not normally be suspected clinically. Immunohistochemistry is needed for substantiation of the morphology and confirmation. We submit this illustrative case report.
2023: Indian Journal of Pathology & Microbiology
https://read.qxmd.com/read/37530366/nodular-glomerulosclerosis-with-crescents-a-double-edged-sword
#9
JOURNAL ARTICLE
Moumita Sengupta, Keya Basu, Arpita Roychowdhury
No abstract text is available yet for this article.
2023: Indian Journal of Pathology & Microbiology
https://read.qxmd.com/read/37530365/warty-dyskeratoma-on-the-scalp-mimicking-keratoacanthoma
#10
JOURNAL ARTICLE
Jae-Ho Lee, Ji-An Uh, Joong-Ho Kim, Soo-Kyung Lee, Myoung-Shin Kim, Un-Ha Lee
No abstract text is available yet for this article.
2023: Indian Journal of Pathology & Microbiology
https://read.qxmd.com/read/37530364/crystal-storing-histiocytosis-forming-a-mass-lesion-in-temporal-lobe
#11
Mine Özşen, Şahsine Tolunay, Hasan Kocaeli, Müfit Parlak
Crystal storing histiocytosis is a disorder characterized by local or diffuse infiltration of histiocytes containing crystalline inclusions. This entity has been reported in several organs, however the involvement of the central nervous system (CNS) is extremely rare and to date only 7 cases of crystal storing histiocytosis (CSH) of CNS have been reported in the English literature. More than 90% patients with CSH had an underlying lymphoproliferative or plasma cell disorders, especially multiple myeloma, lymphoplasmacytic lymphoma or monoclonal gammopathy...
2023: Indian Journal of Pathology & Microbiology
https://read.qxmd.com/read/37530363/primary-orbital-yolk-sac-tumor-in-an-infant-a-rare-entity
#12
Varsha Mishra, Sandeep Jain, Payal Malhotra, Garima Durga, Gauri Kapoor
We report a case of pure orbital yolk sac tumor (YST) in an 11-month-old infant, which is a rare entity. The child presented with progressive painless swelling of the right eye and on examination had proptosis, chemosis, and lid edema. Systemic examination was within normal limits. Magnetic resonance imaging (MRI) orbit revealed a lobulated heterogeneously enhancing right retroocular mass extending up to the orbital apex, displacing the optic nerve and eroding the medial orbital wall. Biopsy of the lesion revealed pure YST histology...
2023: Indian Journal of Pathology & Microbiology
https://read.qxmd.com/read/37530362/anaplastic-undifferentiated-carcinoma-of-pancreas-an-uncommon-variant-diagnosed-on-endoscopic-guided-fine-needle-aspiration
#13
Md Ali Osama, Pooja Bakshi, Kusum Verma
Anaplastic carcinoma of pancreas (ACP) are rare pancreatic neoplasms. They are well known to be associated with more aggressive tumor behavior and less favorable prognosis than usual pancreatic ductal adenocarcinoma. Endoscopic-guided fine needle aspiration (EUS-FNA) is now a widely accepted modality in diagnosis of pancreatic lesions. However, only a few reports are available describing cytological features of anaplastic carcinoma. Here, we report two cases of ACP diagnosed on EUS-FNA.
2023: Indian Journal of Pathology & Microbiology
https://read.qxmd.com/read/37530361/erdheim-chester-disease-misdiagnosed-as-meningioma-of-the-pontocerebellar-angle-a-case-report-and-review-of-literature
#14
Ali Rıza Guvercin, Beyhan Guvercin, Emel Çakır, Uğur Yazar
Erdheim-Chester Disease (ECD) is a rare non-Langerhans form of systemic histiocytosis of unknown etiology with multiple organ involvement. It most commonly affects the long bones, lungs, heart, retroperitoneum, eyes, and kidneys and less commonly the brain and spinal cord. Although there are very few cases of supratentorial ECD mimicking intracranial meningioma reported in literature, to the best of our knowledge, there are no reports on ECD mimicking infratentorial pontocerebellar angle meningioma. The present study reports a case of ECD mimicking pontocerebellar angle meningioma...
2023: Indian Journal of Pathology & Microbiology
https://read.qxmd.com/read/37530360/tumoral-cutaneous-rhinosporidiosis-case-report-and-review-of-literature
#15
Nayantrishna Nath, Santanu Subba, Sanjay K Giri, Priyanka Pant, Aparna Kanungo, Anurag Mishra, Pritinanda Mishra
Rhinosporidiosis is a chronic granulomatous disease caused by Rhinosporidium seeberi commonly affecting nasal mucosa, conjunctiva, and urethra. Subcutaneous tumor nodule presentation is rare and often mimics as sarcoma. Such tumoral rhinosporidiosis has been reported rarely. This report describes a 60-year male who presented with a solitary, firm, nontender swelling in posterior aspect of right leg with an ulcer and mimicking clinically as soft tissue sarcoma. Histopathology was diagnostic. Surgical excision was found to be useful...
2023: Indian Journal of Pathology & Microbiology
https://read.qxmd.com/read/37530359/breast-mass-an-uncommon-clinical-manifestation-of-ovarian-carcinoma-a-case-report-and-brief-literature-review
#16
Nibedita Sahoo, Mohita Ray, Debahuti Mohapatra, Pallak Batalia
Metastasis from non-mammary malignant neoplasms to the breast is rare and represents 0.2%-1.3% of all breast malignancies. Fine needle aspiration cytology (FNAC) is the first line of investigation for any breast lump and cyto-morphological appearance of primary breast malignancies is well documented. Occasionally metastasis to the breast may be the initial presentation and can masquerade clinically as primary breast malignancy. The present case describes the clinical and cytological challenges in an unusual case of ovarian carcinoma with initial presentation as breast mass, mimicking as inflammatory carcinoma...
2023: Indian Journal of Pathology & Microbiology
https://read.qxmd.com/read/37530358/a-rare-case-of-pleuropulmonary-blastoma-type-iii-with-immunohistochemical-study
#17
Siddhi Gaurish Sinai Khandeparkar, Maithili Mandar Kulkarni, Bageshri P Gogate, Chinmayee Sanjeev Dhavan
Here we intend to document a rare case of PPB type III in a 2-year male presenting with an extensive tumor occupying the right hemithorax with immunohistochemical (IHC) study. Pleuropulmonary blastoma (PPB) is a rare variably aggressive, dysodontogenetic, childhood primary intrathoracic malignancy which in up to 25% of cases can be extrapulmonary with attachment to the parietal pleura. It is found in pediatric population under 5 years of age. It was initially proposed as a distinct entity by Manivel et al. in 1988...
2023: Indian Journal of Pathology & Microbiology
https://read.qxmd.com/read/37530357/the-rhabdoid-variant-of-adrenocortical-carcinoma-report-of-three-cases-and-literature-review
#18
Pavithra Ayyanar, Mukund N Sable, Amit K Adhya, Manoj K Das, Madhabananda Kar, Pritinanda Mishra
Adrenocortical carcinoma (ACC) is a rare and aggressive malignancy. Extensive rhabdoid morphology in ACC has been described recently in very few cases. The proportion of rhabdoid morphology and the role of SMARCB1/ INI1 expression in these tumor cells to diagnose the specific variant is not described in the literature. We reviewed the clinicopathological features of nine cases of adrenocortical neoplasm. Out of which, three cases of ACC showed predominant rhabdoid morphology. Large discohesive cells with abundant cytoplasm containing eosinophilic inclusions, eccentric vesicular nucleus, and prominent nucleoli...
2023: Indian Journal of Pathology & Microbiology
https://read.qxmd.com/read/37530356/identification-of-rare-atypical-bcr-abl1-transcript-a-case-report
#19
Jayesh Saha, Vipin Gopinath, Chandran K Nair, Deepak Roshan
CML is characterized by the presence of a BCR-ABL1 fusion transcript. Several guidelines have been published for its detection and molecular monitoring. Here, a case is described of chronic myeloid leukemia presenting in the blast phase with a rare variant transcript, with a discussion on possible red flags in its detection and genetic testing and description of the patient's clinical characteristics. This case highlights the pitfalls of using real-time quantitative reverse-transcription polymerase chain reaction (RQ-PCR) for diagnosis of CML, especially when the clinical picture and the test results are discordant...
2023: Indian Journal of Pathology & Microbiology
https://read.qxmd.com/read/37530355/poems-syndrome-a-rare-entity
#20
Chaganti P Devi, Basimalla R Stephenson, P Ramana Kumari, Panchakarla G Vani, Swargam P Madhooli
POEMS syndrome is a rare paraneoplastic syndrome due to an underlying plasma cell disorder. The diagnosis of POEMS syndrome can be a challenge. A good history, physical examination, and appropriate testing can aid in establishing its diagnosis. We are presenting the case of a 75-year-old man who was diagnosed with POEMS syndrome.
2023: Indian Journal of Pathology & Microbiology
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