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  1. Article ; Online: Immunohistochemical evaluation of biomarkers with predictive role in acromegaly: a literature review.

    Gliga, Maximilian Cosma / Tătăranu, Ligia Gabriela / Popescu, Mihaela / Chinezu, Laura / Paşcanu, Maria Ionela

    Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie

    2023  Volume 64, Issue 1, Page(s) 25–33

    Abstract: Acromegaly is a rare endocrine disorder, which despite the recent advances in diagnosis and management, remains a significant burden in terms of morbidity and mortality for patients because of the frequent aggressive evolution and lack of response to ... ...

    Abstract Acromegaly is a rare endocrine disorder, which despite the recent advances in diagnosis and management, remains a significant burden in terms of morbidity and mortality for patients because of the frequent aggressive evolution and lack of response to available first-line pharmacological therapy. A switch from the classical "trial and error" management to a personalized therapy approach has been proposed through early identification of biomarkers that could predict treatment response and biological behavior. Several such molecular markers have been extensively studied through immunohistochemistry (IHC), among them the somatostatin receptors type 2 (SSTR-2) and type 5 (SSTR-5), which are known to correlate with response to somatostatin analogues treatment, the SSTR-2 negative tumors usually being resistant to first-generation analogues, while SSTR-5 potentially being a predictive marker for the novel agent, Pasireotide. Based on cytokeratin (CK) immunostaining pattern, somatotropinomas have been classified into densely granulated adenomas (DGAs), which present a milder evolution and favorable outcomes after therapy, and sparsely granulated adenomas (SGAs), known to be more aggressive and frequently resistant to first-line treatment options. Other novel markers, such as the E-cadherin cell-adhesion protein, the aryl hydrocarbon receptor-interacting protein (AIP), the cytoskeleton molecule filamin A (FLNA) and the Ki-67 nuclear antigen have also been the highlight of IHC studies on growth hormone (GH)-producing tumors, with promising results regarding their predictive roles for the outcome of acromegalic patients. In this review, we aimed to summarize the current knowledge on the role of IHC for acromegaly, highlighting the most important biomarkers that could offer valuable information for predicting treatment response, biological behavior, and prognosis.
    MeSH term(s) Humans ; Acromegaly ; Adenoma/pathology ; Pituitary Neoplasms ; Biomarkers ; Intracellular Signaling Peptides and Proteins/therapeutic use
    Chemical Substances Biomarkers ; Intracellular Signaling Peptides and Proteins
    Language English
    Publishing date 2023-04-27
    Publishing country Romania
    Document type Review ; Journal Article
    ZDB-ID 1062519-7
    ISSN 2066-8279 ; 1220-0522 ; 0035-4007
    ISSN (online) 2066-8279
    ISSN 1220-0522 ; 0035-4007
    DOI 10.47162/RJME.64.1.03
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Successful Pregnancy in a Patient with Long-Standing Acromegaly – a Case Report

    Gliga Maximilian Cosma / Pașcanu Maria Ionela / Gliga Camelia / Réti Zsuzsanna

    Journal of Interdisciplinary Medicine, Vol 5, Iss 3, Pp 114-

    2020  Volume 119

    Abstract: Introduction: Acromegaly is a rare endocrine disorder of the growth hormone (GH)-insulin-like growth factor 1 (IGF1) metabolism that can affect women of fertile age. Although uncommon, pregnancies in acromegalic women can occur, with data regarding the ... ...

    Abstract Introduction: Acromegaly is a rare endocrine disorder of the growth hormone (GH)-insulin-like growth factor 1 (IGF1) metabolism that can affect women of fertile age. Although uncommon, pregnancies in acromegalic women can occur, with data regarding the management of these cases being very limited, mostly consisting of case reports.
    Keywords acromegaly ; pregnancy ; treatment ; Medicine ; R
    Language English
    Publishing date 2020-09-01T00:00:00Z
    Publisher Sciendo
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article: Ectopic intracavernous corticotroph microadenoma: case report of an extremely rare pathology.

    Bălaşa, Adrian Florian / Chinezu, Rareş / Teleanu, Daniel Mihai / Paşcanu, Maria Ionela / Chinezu, Laura / Borda, Angela

    Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie

    2018  Volume 58, Issue 4, Page(s) 1447–1451

    Abstract: Ectopic pituitary adenomas (EPAs) are most likely tumors developing from the cellular remnants following the migration of Rathke's pouch. We present the case of a 54-year-old female diagnosed with Cushing's syndrome. Magnetic resonance imaging (MRI) ... ...

    Abstract Ectopic pituitary adenomas (EPAs) are most likely tumors developing from the cellular remnants following the migration of Rathke's pouch. We present the case of a 54-year-old female diagnosed with Cushing's syndrome. Magnetic resonance imaging (MRI) identified an ectopic microadenoma located in the median wall of the cavernous sinus. Microscopic transsphenoidal surgery was performed and the lesion was completely removed without any postoperative surgical complications. Based on characteristic microscopic and immunohistochemical features and on recent clinicopathological prognostic classifications, the histopathological diagnosis was non-proliferative, non-invasive corticotroph pituitary neuroendocrine tumor, grade 1a. Complete remission of disease was achieved postoperatively and was maintained for one year following surgery. MRI showed complete resection, without tumor recurrence at one and two years. Occurrence of an ectopic intracavenous adrenocorticotropic hormone (ACTH)-secreting adenoma is extremely rare and poses difficulties both in the identification, surgery, histopathological grading, and adequate endocrinological treatment and follow-up.
    MeSH term(s) Adenoma/pathology ; Corticotrophs/pathology ; Female ; Humans ; Middle Aged ; Pituitary Neoplasms/complications
    Language English
    Publishing date 2018-03-16
    Publishing country Romania
    Document type Case Reports ; Journal Article
    ZDB-ID 1062519-7
    ISSN 2066-8279 ; 1220-0522 ; 0035-4007
    ISSN (online) 2066-8279
    ISSN 1220-0522 ; 0035-4007
    Database MEDical Literature Analysis and Retrieval System OnLINE

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