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  1. Article: Wuchereria bancrofti

    Prasoon, Dev / Agrawal, Parimal

    Journal of cytology

    2020  Volume 37, Issue 4, Page(s) 182–188

    Abstract: Background: Wuchereriasis is a significant cause of chronic morbidity. It can affect any organ/tissue in the body. Fine-needle aspiration cytology (FNAC) is an easy method for its detection. A comprehensive analysis of the various facets involved has ... ...

    Abstract Background: Wuchereriasis is a significant cause of chronic morbidity. It can affect any organ/tissue in the body. Fine-needle aspiration cytology (FNAC) is an easy method for its detection. A comprehensive analysis of the various facets involved has not been discussed in detail in any publication.
    Materials and methods: A twenty-six year (February 1994 to January 2020) retrospective audit of all patients who were cytologically diagnosed with wuchereriasis was performed. Data regarding age, sex, organ/tissue involved, and presence of co-existing disease were noted. Hematoxylin and eosin (H and E) and May-Grünwald-Giemsa (MGG) stained slides were screened for microfilaria, adult worm, larval forms, microfilaria ghosts, epithelioid cell granuloma, and eosinophils.
    Results: Audit yielded 19,323 cases of which 110 had wuchereriasis giving an incidence of 0.57%. The 11-30 year age group accounted for 41.8% cases. Male: female ratio was 1.04:1. Duration of disease at presentation ranged from 3 days to 24 years. Lymph node was the commonest site involved (40%), followed by soft tissue (23.6%) and female breast (14.5%). Highest parasitic load was encountered in female breast aspirates. Microfilaria bancrofti was seen in 105 (95.4%) cases. In the five cases where microfilaria bancrofti was not encountered, diagnosis was established by the presence of adult gravid female worm (2 cases), coiled larvae (2 cases), and both adult gravid female worm and coiled larvae (1 case). Microfilaria ghosts were seen in 18.2% cases. Coexisting benign and malignant diseases were encountered in 17.3% and 13.6% cases, respectively.
    Conclusion: FNAC provides a simple and inexpensive means of detecting wuchereriasis and is preferred over histopathology. All stages of development of this nematode in human beings are identified in cytology. Microfilaria ghost is a useful clue in screening. The presence of granuloma and eosinophilic infiltrate indicates tissue reaction only. Patients with asymptomatic microfilaraemia should be reported in cytology as they merit treatment.
    Language English
    Publishing date 2020-09-16
    Publishing country India
    Document type Journal Article
    ZDB-ID 645018-0
    ISSN 0970-9371
    ISSN 0970-9371
    DOI 10.4103/JOC.JOC_59_20
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Scurvy Masquerading as Septic Arthritis in a Case of Cerebral Palsy.

    Jain, Deepak S / Agrawal, Tushar / Malviya, Parimal K

    Journal of orthopaedic case reports

    2021  Volume 11, Issue 8, Page(s) 107–110

    Abstract: Introduction: Scurvy is a rarely seen in pediatric patients nowadays, seen more in those with developmental delay, autism or those who are severely malnourished. Epiphyseal separations are known to occur in scurvy, but only a few such cases have been ... ...

    Abstract Introduction: Scurvy is a rarely seen in pediatric patients nowadays, seen more in those with developmental delay, autism or those who are severely malnourished. Epiphyseal separations are known to occur in scurvy, but only a few such cases have been reported in children with cerebral palsy. The diagnosis is often misleading since other morbidities as trauma, malignancies, coagulopathies, septic arthritis, osteomyelitis, or rheumatologic disorders are often considered at first. We report the case of 4-year-old female child with cerebral palsy in whom the initial concern was septic arthritis/osteomyelitis based upon clinical presentation, ultrasonic and magnetic resonance imaging, led to a surgery revealing subperiosteal hematomas.
    Case report: A 4-year-old girl was admitted in the pediatrics department for fever and bilateral knee joint pain for 3 days. She was a diagnosed case of with cerebral palsy, psyco-developmental delay, and epileptogenic disorder put under valproic acid. She was toxic and febrile. Within 4 h after admission, both knees developed tense shiny intense swelling associated with pain, redness, and local rise of temperature with limited active range of motion. Near-complete passive range of motion was noted. There were no abnormal findings on the rest of the musculoskeletal examination. Aspiration of the knee revealed subperiosteal hematoma diagnostic of scurvy.
    Conclusion: Scurvy is exceedingly rare in children nowadays; however, its presentation among risky populations should not be forgotten. Musculoskeletal revelations, mostly subperiosteal hematoma, are the main manifestation of scurvy in the pediatric population. Scurvy as a differential diagnosis for trauma, osteomyelitis, septic arthritis will always be a bane for orthopedic surgeons. A heightened awareness is needed to avoid unnecessary surgery, unnecessary tests, and procedures and to be able to start treatment for a potentially fatal but easily curable disease.
    Language English
    Publishing date 2021-12-17
    Publishing country India
    Document type Case Reports
    ZDB-ID 2658169-3
    ISSN 2250-0685
    ISSN 2250-0685
    DOI 10.13107/jocr.2021.v11.i08.2388
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: An unusual etiology of plummer-Vinson syndrome.

    Jain, Ankur / Agrawal, Parimal / Malhotra, Pankaj / Nada, Ritambhra / Varma, Subhash

    Blood research

    2018  Volume 53, Issue 1, Page(s) 79–81

    Language English
    Publishing date 2018-03-27
    Publishing country Korea (South)
    Document type Journal Article
    ZDB-ID 2711910-5
    ISSN 2288-0011 ; 2287-979X
    ISSN (online) 2288-0011
    ISSN 2287-979X
    DOI 10.5045/br.2018.53.1.79
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Renal and Pulmonary Dense Deposit Disease Presenting as Pulmonary-Renal Syndrome.

    Nada, Ritambhra / Kumar, Ashwani / Agrawal, Parimal / Ramachandran, Raja / Sethi, Sanjeev

    Kidney international reports

    2018  Volume 3, Issue 3, Page(s) 755–761

    Language English
    Publishing date 2018-01-31
    Publishing country United States
    Document type Case Reports
    ISSN 2468-0249
    ISSN (online) 2468-0249
    DOI 10.1016/j.ekir.2018.01.005
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Extraventricular neurocytoma: An uncommon tumor in a young boy. A review of literature.

    Agrawal, Parimal / Gupta, Kirti / Sodhi, Harsimrat B S

    Neurology India

    2017  Volume 65, Issue 1, Page(s) 202–205

    MeSH term(s) Brain Neoplasms/diagnosis ; Brain Neoplasms/pathology ; Child ; Humans ; Male ; Neurocytoma/diagnosis ; Neurocytoma/pathology ; Peptides, Cyclic
    Chemical Substances MTI-101 ; Peptides, Cyclic
    Language English
    Publishing date 2017-03-21
    Publishing country India
    Document type Case Reports ; Letter ; Review
    ZDB-ID 415522-1
    ISSN 1998-4022 ; 0028-3886
    ISSN (online) 1998-4022
    ISSN 0028-3886
    DOI 10.4103/0028-3886.198201
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Extraventricular neurocytoma

    Parimal Agrawal / Kirti Gupta / Harsimrat B S Sodhi

    Neurology India, Vol 65, Iss 1, Pp 202-

    An uncommon tumor in a young boy. A review of literature

    2017  Volume 205

    Keywords Neurology. Diseases of the nervous system ; RC346-429 ; Neurosciences. Biological psychiatry. Neuropsychiatry ; RC321-571 ; Internal medicine ; RC31-1245 ; Medicine ; R
    Language English
    Publishing date 2017-01-01T00:00:00Z
    Publisher Medknow Publications
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article ; Online: Renal actinomycosis.

    Agrawal, Parimal / Vaiphei, Kim

    BMJ case reports

    2014  Volume 2014

    Abstract: Actinomycosis of the kidney is rare and less than 50 cases have been reported in the English literature. Reported presentations are pyelonephritis, renal abscesses or pyonephrosis. To date, one case of actinomycosis associated necrotising papillitis has ... ...

    Abstract Actinomycosis of the kidney is rare and less than 50 cases have been reported in the English literature. Reported presentations are pyelonephritis, renal abscesses or pyonephrosis. To date, one case of actinomycosis associated necrotising papillitis has been reported. We describe the second case of such a rare association of actinomycosis with papillary necrosis.
    MeSH term(s) Actinomyces ; Actinomycosis/complications ; Actinomycosis/microbiology ; Humans ; Inflammation/microbiology ; Kidney/microbiology ; Kidney/pathology ; Kidney Medulla/microbiology ; Kidney Medulla/pathology ; Kidney Papillary Necrosis/etiology ; Kidney Papillary Necrosis/microbiology ; Male ; Middle Aged
    Language English
    Publishing date 2014-11-18
    Publishing country England
    Document type Case Reports ; Journal Article
    ISSN 1757-790X
    ISSN (online) 1757-790X
    DOI 10.1136/bcr-2014-205892
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Correlation of eosinophilic structures with detection of acid-fast bacilli in fine needle aspiration smears from tuberculous lymph nodes

    Dev Prasoon / Parimal Agrawal

    Journal of Cytology, Vol 31, Iss 3, Pp 149-

    Is eosinophilic structure the missing link in spectrum of tuberculous lesion?

    2014  Volume 153

    Abstract: Background: Acid-fast bacilli (AFB) is not seen in all necrotic tuberculous lesions. If the subset of tuberculous lesions which yield positive result for AFB can be identified, it would save on time and manpower besides optimizing use of resources. A ... ...

    Abstract Background: Acid-fast bacilli (AFB) is not seen in all necrotic tuberculous lesions. If the subset of tuberculous lesions which yield positive result for AFB can be identified, it would save on time and manpower besides optimizing use of resources. A prospective study was undertaken to assess if presence of eosinophilic structures (ESs) in necrotic tuberculous lesions correlated with the presence of AFB. Materials and Methods: Patients referred for fine needle aspiration cytology for evaluation of lymphadenopathy between July 2012 and June 2013 were analyzed. The hematoxylin and eosin and May-Grünwald-Giemsa stained slides were screened for epithelioid cell granuloma, ES and necrosis and Ziehl Neelsen stained smears for AFB. Result: One hundred and eight tuberculous lymph nodes yielded necrotic material on aspiration. Four cytologic pictures were seen: (a) ES + AFB + in 58.33%, (b) ES + AFB− in 20.37%, (c) ES− AFB + in 9.26% (d) ES− AFB− in 12.04% cases. Overall AFB was found in 67.59% cases, out of which 58.33% correlated with the presence of ES while 9.26% were seen in smears without ES. Conclusion: Presence of ESs should be included in the morphological description of tuberculous lesions. In the absence of granulomas, they indicate tuberculous nature of the lesion. Presence of ES mandates a search for AFB as probability of finding AFB is high in such lesions. Significance of ES lies in their presence and not in their absence. Eosinophilic structures appear to be the missing link in the spectrum of tuberculous lesion.
    Keywords Acid fast bacilli; eosinophilic structures; fine needle aspiration cytology; tuberculosis ; Cytology ; QH573-671 ; Biology (General) ; QH301-705.5 ; Science ; Q
    Subject code 630
    Language English
    Publishing date 2014-01-01T00:00:00Z
    Publisher Medknow Publications
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  9. Article: Correlation of eosinophilic structures with detection of acid-fast bacilli in fine needle aspiration smears from tuberculous lymph nodes: Is eosinophilic structure the missing link in spectrum of tuberculous lesion?

    Prasoon, Dev / Agrawal, Parimal

    Journal of cytology

    2014  Volume 31, Issue 3, Page(s) 149–153

    Abstract: Background: Acid-fast bacilli (AFB) is not seen in all necrotic tuberculous lesions. If the subset of tuberculous lesions which yield positive result for AFB can be identified, it would save on time and manpower besides optimizing use of resources. A ... ...

    Abstract Background: Acid-fast bacilli (AFB) is not seen in all necrotic tuberculous lesions. If the subset of tuberculous lesions which yield positive result for AFB can be identified, it would save on time and manpower besides optimizing use of resources. A prospective study was undertaken to assess if presence of eosinophilic structures (ESs) in necrotic tuberculous lesions correlated with the presence of AFB.
    Materials and methods: Patients referred for fine needle aspiration cytology for evaluation of lymphadenopathy between July 2012 and June 2013 were analyzed. The hematoxylin and eosin and May-Grünwald-Giemsa stained slides were screened for epithelioid cell granuloma, ES and necrosis and Ziehl Neelsen stained smears for AFB.
    Result: One hundred and eight tuberculous lymph nodes yielded necrotic material on aspiration. Four cytologic pictures were seen: (a) ES(+) AFB(+) in 58.33%, (b) ES(+) AFB(-) in 20.37%, (c) ES(-) AFB(+) in 9.26% (d) ES(-) AFB(-) in 12.04% cases. Overall AFB was found in 67.59% cases, out of which 58.33% correlated with the presence of ES while 9.26% were seen in smears without ES.
    Conclusion: Presence of ESs should be included in the morphological description of tuberculous lesions. In the absence of granulomas, they indicate tuberculous nature of the lesion. Presence of ES mandates a search for AFB as probability of finding AFB is high in such lesions. Significance of ES lies in their presence and not in their absence. Eosinophilic structures appear to be the missing link in the spectrum of tuberculous lesion.
    Language English
    Publishing date 2014-12-23
    Publishing country India
    Document type Journal Article
    ZDB-ID 645018-0
    ISSN 0970-9371
    ISSN 0970-9371
    DOI 10.4103/0970-9371.145647
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Complement factor H gene polymorphisms and vivax malaria associated thrombotic microangiopathy

    Parimal Agrawal / Ashwani Kumar / Amber Parwaiz / Amit Rawat / Karalanglin Tiewsoh / Ritambhra Nada

    Saudi Journal of Kidney Diseases and Transplantation, Vol 30, Iss 2, Pp 540-

    2019  Volume 544

    Abstract: Acute kidney injury (AKI) occurs in about 1% of cases of malaria; however, in these cases, the mortality rate can be as high as 45%. Thrombotic microangiopathy (TMA) as a cause of AKI in malaria is rare with only a handful cases documented in literature ... ...

    Abstract Acute kidney injury (AKI) occurs in about 1% of cases of malaria; however, in these cases, the mortality rate can be as high as 45%. Thrombotic microangiopathy (TMA) as a cause of AKI in malaria is rare with only a handful cases documented in literature so far. Alternate complement pathway (ACP) dysregulation as a major mechanism of injury in the development of thrombotic microangiopathies is well known. It is proposed that patients with preexisting defects in ACP are usually clinically silent, until stress condition such as infections help manifest them. Herein, we describe the presence of two complement factor H (CFH) variants in an 8-year-old female with vivax malaria associated TMA. The complement workup confirmed dysregulated ACP and revealed two single-nucleotide polymorphisms in CFH gene, i.e. exon-7 rs1061147 (p.Ala243Ala) and exon-9 rs1061170 (p.His402Tyr) which predisposed this patient to develop TMA precipitated by vivax malaria.
    Keywords Medicine ; R
    Subject code 616
    Language English
    Publishing date 2019-01-01T00:00:00Z
    Publisher Wolters Kluwer Medknow Publications
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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