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  1. Article: Solitary Extramedullary Plasmacytoma of Nasal Cavity.

    Mishra, Utkal Priyadarshi / Verma, Ashish Kumar / Chaurasia, Jai Kumar

    Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India

    2023  Volume 75, Issue 4, Page(s) 4060–4065

    Abstract: Solitary extramedullary plasmacytoma (SEP) of the nasal cavity is a rare neoplastic condition characterized by the localized proliferation of abnormal plasma cells. We present a case of SEP involving the nasal cavity in a 40-year-old male patient who ... ...

    Abstract Solitary extramedullary plasmacytoma (SEP) of the nasal cavity is a rare neoplastic condition characterized by the localized proliferation of abnormal plasma cells. We present a case of SEP involving the nasal cavity in a 40-year-old male patient who presented with nasal obstruction and recurrent epistaxis. The diagnosis was confirmed through clinical evaluation, imaging studies, and histopathological examination of excised specimen. The patient underwent trans-nasal endoscopic excision of nasal mass without any adjuvant therapy, which resulted in successful local control. This case report highlights the clinical presentation, diagnostic approach, treatment modalities, and favourable prognosis associated with solitary extramedullary plasmacytoma of the nasal cavity.
    Language English
    Publishing date 2023-07-10
    Publishing country India
    Document type Journal Article
    ZDB-ID 1471137-0
    ISSN 0973-7707 ; 2231-3796 ; 0019-5421
    ISSN (online) 0973-7707
    ISSN 2231-3796 ; 0019-5421
    DOI 10.1007/s12070-023-04061-0
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  2. Article ; Online: Sporotrichoid spread of locoregional bacille Calmette-Guerin infection following intralesional immunotherapy for verruca vulgaris in an immunocompetent adult.

    Patra, Suman / Maninder, Kaur / Soumya, Narula / Dinesh, P Asati / Jai Kumar, Chaurasia

    Indian journal of dermatology, venereology and leprology

    2023  Volume 89, Issue 5, Page(s) 733–735

    MeSH term(s) Adult ; Humans ; BCG Vaccine ; Immunotherapy/adverse effects ; Urinary Bladder Neoplasms ; Warts/diagnosis ; Warts/drug therapy
    Chemical Substances BCG Vaccine
    Language English
    Publishing date 2023-05-19
    Publishing country United States
    Document type Letter
    ZDB-ID 416068-x
    ISSN 0973-3922 ; 0019-5162 ; 0378-6323
    ISSN (online) 0973-3922
    ISSN 0019-5162 ; 0378-6323
    DOI 10.25259/IJDVL_964_20
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  3. Article: Role of cytopathology in diagnosing phaeohyphomycosis masquerading as nerve abscess in a lepromatous leprosy patient: A case report.

    Yadav, Shakti Kumar / Chandana, B K / Panwar, Hemlata / Chaurasia, Jai Kumar / Jayashankar, E / Asati, Dinesh

    International journal of surgery case reports

    2023  Volume 110, Page(s) 108741

    Abstract: Introduction and importance: Phaeohyphomycosis is a rare fungal infection primarily affecting immunocompromised individuals. Its clinical manifestations are diverse, and diagnosis can be challenging, particularly when lesions mimic other conditions.: ... ...

    Abstract Introduction and importance: Phaeohyphomycosis is a rare fungal infection primarily affecting immunocompromised individuals. Its clinical manifestations are diverse, and diagnosis can be challenging, particularly when lesions mimic other conditions.
    Case presentation: A 66-year-old male, with a history of irregular leprosy treatment and prolonged steroid use, presented with symptoms suggestive of a nerve abscess. On examination, cystic swellings were observed on the left thumb and leg. Histopathological examination and fine needle aspiration cytology (FNAC) revealed melanized hyphae, leading to a final diagnosis of phaeohyphomycosis. The patient was treated with oral itraconazole, leading to regression in lesion size.
    Clinical discussion: Leprosy patients on long-term steroids are especially susceptible. The pathogenicity of these fungi in immunocompetent people is believed to be due to melanin in their cell walls, which defends against host defenses. Diagnosis involves histopathological examinations, staining, and fungal culture. Treatment involves surgical excision and antifungal drugs. If untreated, it can lead to severe complications including fatal brain infections.
    Conclusion: This case highlights the unusual presentation of phaeohyphomycosis mimicking a nerve abscess in a leprosy patient. It underscores the importance of a high degree of clinical suspicion in diagnosing such rare infections, particularly in immunocompromised individuals. It also emphasizes the value of FNAC in reaching a definitive diagnosis. Prompt diagnosis and appropriate treatment are essential to prevent potentially serious outcomes.
    Language English
    Publishing date 2023-08-29
    Publishing country Netherlands
    Document type Case Reports
    ISSN 2210-2612
    ISSN 2210-2612
    DOI 10.1016/j.ijscr.2023.108741
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  4. Article: Circumscribed Area of Leukotrichia over Plexiform Neurofibroma: An Important Clue or Mere Coincidence?

    Sahni, Mukesh K / Chaurasia, Jai Kumar / Patra, Suman

    Indian dermatology online journal

    2020  Volume 11, Issue 5, Page(s) 831–832

    Language English
    Publishing date 2020-09-19
    Publishing country India
    Document type Journal Article
    ZDB-ID 2585814-2
    ISSN 2249-5673 ; 2229-5178
    ISSN (online) 2249-5673
    ISSN 2229-5178
    DOI 10.4103/idoj.IDOJ_606_19
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  5. Article: Hypoplastic coronary artery disease, as a cause of sudden death.

    Sangita, Moirangthem / Yadav, Jayanthi / Chaurasia, Jai Kumar / Arora, Arneet / Jahan, Afsar / Patnaik, Mrinal

    Autopsy & case reports

    2023  Volume 13, Page(s) e2023440

    Abstract: Hypoplastic coronary artery disease (HCAD) is a rare coronary artery anomaly that may be the cause of sudden death. It can involve a single or all coronary arteries. This anomaly may cause circulatory insufficiency leading to myocardial infarction. HCAD ... ...

    Abstract Hypoplastic coronary artery disease (HCAD) is a rare coronary artery anomaly that may be the cause of sudden death. It can involve a single or all coronary arteries. This anomaly may cause circulatory insufficiency leading to myocardial infarction. HCAD has no symptoms or may exhibit cardiovascular signs like syncope, dyspnea, chest discomfort, or dizziness. It is often diagnosed at autopsy, and early diagnosis is made with a coronary angiogram. We report HCAD as the cause of the sudden death of a 25-year-old female with a history of loss of consciousness following exertion. On autopsy, all the coronary arteries' lumen was narrowed with thin vessel walls. Histopathological examination shows an underdeveloped and missing muscular layer of the left anterior descending and circumflex coronary arteries' vascular wall. Many cases of HCAD diagnosed by radiographic imaging in living patients have been reported in the literature, but a structural anomaly of coronaries leading to HCAD has not been reported. We report a case of HCAD describing the histopathological examination findings of the vascular wall of coronary vessels illustrating the structural difference.
    Language English
    Publishing date 2023-07-19
    Publishing country Brazil
    Document type Case Reports
    ZDB-ID 2815488-5
    ISSN 2236-1960
    ISSN 2236-1960
    DOI 10.4322/acr.2023.440
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  6. Article ; Online: Unusual coexistence of Stewart-Treves syndrome and sickle cell anaemia: a case of dual pathology.

    Walke, Vaishali A / Datar, Sonali / Kowe, Balwant / Chaurasia, Jai Kumar

    BMJ case reports

    2022  Volume 15, Issue 7

    Abstract: Chronic lymphoedema can rarely be complicated by an angiosarcoma. This combination called Stewart-Treves syndrome usually observed in upper limb in patients of post-mastectomy with axillary lymph node resection. Here, we report a male patient who had a ... ...

    Abstract Chronic lymphoedema can rarely be complicated by an angiosarcoma. This combination called Stewart-Treves syndrome usually observed in upper limb in patients of post-mastectomy with axillary lymph node resection. Here, we report a male patient who had a 10-year history of right leg elephantiasis. Later on, he developed two large ulceronodular masses in the same leg with few satellite nodules in the surrounding skin. With the clinical suspicion of malignancy, a wedge biopsy was performed which revealed histological features of angiosarcoma with sickled red cells. The above knee amputation specimen received further confirmed the histological diagnosis. The investigation for haemoglobinopathy also suggested the presence of sickle cell trait. This report describes a multifocal tumour as a rare manifestation of Stewart-Treves syndrome in a post-filariasis case with sickle cell trait, which is an extremely uncommon combination.
    MeSH term(s) Anemia, Sickle Cell/complications ; Breast Neoplasms/surgery ; Hemangiosarcoma/diagnosis ; Humans ; Lymphangiosarcoma ; Male ; Mastectomy/adverse effects ; Sickle Cell Trait/complications ; Syndrome
    Language English
    Publishing date 2022-07-06
    Publishing country England
    Document type Case Reports ; Journal Article
    ISSN 1757-790X
    ISSN (online) 1757-790X
    DOI 10.1136/bcr-2022-249379
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  7. Article ; Online: Cytological diagnosis of sclerosing adenosis of breast: Diagnostic challenges and literature review.

    Sharma, Tanya / Chaurasia, Jai Kumar / Kumar, Vinay / Mukhopadhyay, Sramana / Joshi, Deepti

    Cytopathology : official journal of the British Society for Clinical Cytology

    2021  Volume 32, Issue 6, Page(s) 827–830

    Language English
    Publishing date 2021-08-03
    Publishing country England
    Document type Case Reports ; Journal Article
    ZDB-ID 1034190-0
    ISSN 1365-2303 ; 0956-5507 ; 1350-4037
    ISSN (online) 1365-2303
    ISSN 0956-5507 ; 1350-4037
    DOI 10.1111/cyt.13041
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  8. Article: Tolosa Hunt Syndrome: A Challenging Diagnosis from Otorhinolaryngologist Perspective-A Case Report.

    Behera, Ganakalyan / Gupta, Vikas / Mishra, Utkal P / Chaurasia, Jai Kumar

    Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India

    2021  Volume 74, Issue Suppl 3, Page(s) 5681–5684

    Abstract: Tolosa Hunt syndrome is a rare disorder characterized by idiopathic chronic granulomatous lesion involving cavernous sinus. The presenting symptoms are severe frontal headache, periorbital pain, ptosis, and diplopia. Usually, patients with headache and ... ...

    Abstract Tolosa Hunt syndrome is a rare disorder characterized by idiopathic chronic granulomatous lesion involving cavernous sinus. The presenting symptoms are severe frontal headache, periorbital pain, ptosis, and diplopia. Usually, patients with headache and ptosis primarily visit neurologists or ophthalmologists. Only when imaging reveals any intracranial lesion involving paranasal sinuses, these patients get referred to otorhinolaryngologists. We would like to describe here the challenges we faced as otorhinolaryngologist, in diagnosis and management of a case of painful ophthalmoplegia as Tolosa Hunt Syndrome. A 55-year-old male presented to us with complaints of left frontal headache, periorbital pain, diplopia, and ptosis of left eye. Imaging and endoscopic biopsy revealed granulomatous lesion involving cavernous sinus with no evidence of fungal aetiology. Patient responded well to systemic steroid therapy with complete resolution of symptoms and no remission till two years of follow up. Tolosa Hunt Syndrome remains a diagnosis of exclusion. Trans-nasal endoscopic biopsy in selected cases may be contributory to the diagnosis. It responds well to systemic steroid therapy. Although chances of relapse are there yet prognosis is excellent.
    Language English
    Publishing date 2021-11-29
    Publishing country India
    Document type Journal Article
    ZDB-ID 1471137-0
    ISSN 0973-7707 ; 2231-3796 ; 0019-5421
    ISSN (online) 0973-7707
    ISSN 2231-3796 ; 0019-5421
    DOI 10.1007/s12070-021-02992-0
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  9. Article: Novel Insights into Understanding the Molecular Dialogues between Bipolaroxin and the Gα and Gβ Subunits of the Wheat Heterotrimeric G-Protein during Host-Pathogen Interaction.

    Malviya, Deepti / Singh, Udai B / Dehury, Budheswar / Singh, Prakash / Kumar, Manoj / Singh, Shailendra / Chaurasia, Anurag / Yadav, Manoj Kumar / Shankar, Raja / Roy, Manish / Rai, Jai P / Mukherjee, Arup K / Solanki, Ishwar Singh / Kumar, Arun / Kumar, Sunil / Singh, Harsh V

    Antioxidants (Basel, Switzerland)

    2022  Volume 11, Issue 9

    Abstract: Spot blotch disease of wheat, caused by the ... ...

    Abstract Spot blotch disease of wheat, caused by the fungus
    Language English
    Publishing date 2022-09-05
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2704216-9
    ISSN 2076-3921
    ISSN 2076-3921
    DOI 10.3390/antiox11091754
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  10. Article ; Online: Invasive fungal disease of the central nervous system: Challenging diagnosis of a rare fungus by intraoperative squash cytology.

    Chaurasia, Jai Kumar / Naik, Bitan / Tandon, Ashwani / Tadepalli, Karuna / Khurana, Ujjawal / Kapoor, Neelkamal

    Cytopathology : official journal of the British Society for Clinical Cytology

    2020  Volume 32, Issue 3, Page(s) 353–355

    MeSH term(s) Adult ; Central Nervous System/microbiology ; Cytodiagnosis/methods ; Cytological Techniques/methods ; Fungi/pathogenicity ; Humans ; Male ; Mycoses/diagnosis ; Mycoses/microbiology ; Mycoses/pathology
    Language English
    Publishing date 2020-11-30
    Publishing country England
    Document type Case Reports
    ZDB-ID 1034190-0
    ISSN 1365-2303 ; 0956-5507 ; 1350-4037
    ISSN (online) 1365-2303
    ISSN 0956-5507 ; 1350-4037
    DOI 10.1111/cyt.12933
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