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  1. Article: Cytomorphologic Attributes of Epithelial Myoepithelial Carcinoma of Nasal Cavity - A Rare Tumor with Unusual Clinical Presentation.

    Amita, Krishnappa / Vijayshankar, Shivshankar / Abhishek, M G / Kumari, Amita

    Journal of clinical and diagnostic research : JCDR

    2016  Volume 10, Issue 9, Page(s) ED10–ED12

    Abstract: Epithelial-Myoepithelial Carcinoma (EMC) is a rare low grade epithelial malignancy of major Salivary Glands (SG). Though the histomorphology of this tumor is distinct, unusual location and clinical presentation may pose diagnostic difficulties especially ...

    Abstract Epithelial-Myoepithelial Carcinoma (EMC) is a rare low grade epithelial malignancy of major Salivary Glands (SG). Though the histomorphology of this tumor is distinct, unusual location and clinical presentation may pose diagnostic difficulties especially when this lesion is first encountered at cytology. We report a case of 60-year-old female presenting with nasal obstruction of three months duration. At FNAC the diagnosis of EMC was suggested and it was confirmed on histopathology. We present this case highlighting the cytomorphologic attributes of this rare tumor occurring at an extremely uncommon location - Nasal cavity.
    Language English
    Publishing date 2016-09-01
    Publishing country India
    Document type Case Reports
    ZDB-ID 2775283-5
    ISSN 0973-709X ; 2249-782X
    ISSN (online) 0973-709X
    ISSN 2249-782X
    DOI 10.7860/JCDR/2016/20538.8571
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Cytohistologically Diagnosed Giant Intramammary Epidermal Inclusion Cyst- An Interesting Breast Carcinoma Mimic

    Hemalatha. A. L / Abhishek. M.G / Vijay Shankar. S / Anoosha. K / Ashok. K. P

    National Journal of Laboratory Medicine, Vol 4, Iss 1, Pp 11-

    2015  Volume 13

    Abstract: Epidermal inclusion cyst arising from the breast is a very interesting, rare, benign and diagnostically challenging condition since it may easily be mistaken clinically for malignancy, thereby creating undue anxiety and apprehension until the definitive ... ...

    Abstract Epidermal inclusion cyst arising from the breast is a very interesting, rare, benign and diagnostically challenging condition since it may easily be mistaken clinically for malignancy, thereby creating undue anxiety and apprehension until the definitive diagnosis is formulated. Epidermal inclusion cyst results due to proliferation and implantation of epidermal elements which get compartmentalized as cysts within the dermis. The common sites of occurrence include face, trunk, extremities and scalp. But, epidermal inclusion cysts of the breast are rare. They deserve attention and importance since they may be misdiagnosed as malignant breast neoplasms both on clinical and radiological examination. Fine Needle Aspiration Cytology (FNAC) and histopathological examination play a pivotal role in their diagnosis and management. We report a case of a huge epidermal inclusion cyst of the breast occurring in a 55 year old female which was clinically and radiologically diagnosed as breast abscess and referred for evaluation to rule out malignancy. A definitive opinion of epidermal inclusion cyst was offered on FNA since the aspirate had the classic gross and microscopic features. Considering the huge size of the breast mass, a complete cyst excision was performed and the cytodiagnosis was confirmed by histopathological examination.
    Keywords epidermal inclusion cyst ; follicular infundibular cyst ; intramammary ; Microbiology ; QR1-502 ; Chemistry ; QD1-999
    Subject code 610
    Language English
    Publishing date 2015-01-01T00:00:00Z
    Publisher JCDR Research and Publications Pvt. Ltd.
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    Full text online

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  3. Article: Placental site trophoblastic tumour: a case report.

    Hemalatha, A L / Kumar, Deepak B / Sumanth, D / Abhishek, M G / Shashidhar, H B

    Indian journal of pathology & microbiology

    2007  Volume 50, Issue 3, Page(s) 581–583

    Abstract: Placental site trophoblastic tumour (PSTT) is a rare form of trophoblastic disease accounting for < 2% of all gestational trophoblastic neoplasms. Most of the cases follow a normal pregnancy and a small number have a preceeding molar pregnancy or ... ...

    Abstract Placental site trophoblastic tumour (PSTT) is a rare form of trophoblastic disease accounting for < 2% of all gestational trophoblastic neoplasms. Most of the cases follow a normal pregnancy and a small number have a preceeding molar pregnancy or spontaneous abortion. It can occur as early as several weeks or as late as 15 years after normal delivery, molar pregnancy or abortion. Excessive intermediate trophoblastic activity is the most important diagnostic criterion of this tumour originating from non villous trophoblast. But the possibility of a PSTT should be considered when there is excessive intermediate trophoblastic activity despite the presence of chorionic villi as in the present case. This case report highlights the unusual features like rarity of the tumour (< 2%), occurrence following spontaneous abortion which happens only in a minority of cases, and presence of chorionic villi in the tumour despite the fact that the tumour is of non villous trophoblastic origin.
    MeSH term(s) Abortion, Spontaneous/pathology ; Adult ; Female ; Humans ; Pregnancy ; Trophoblastic Tumor, Placental Site/diagnosis ; Trophoblastic Tumor, Placental Site/etiology ; Trophoblastic Tumor, Placental Site/pathology ; Trophoblasts/pathology ; Uterine Neoplasms/diagnosis ; Uterine Neoplasms/etiology ; Uterine Neoplasms/pathology
    Language English
    Publishing date 2007-07
    Publishing country India
    Document type Case Reports ; Journal Article
    ZDB-ID 197621-7
    ISSN 0974-5130 ; 0377-4929
    ISSN (online) 0974-5130
    ISSN 0377-4929
    Database MEDical Literature Analysis and Retrieval System OnLINE

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