Rosa Maria Ríos-pelegrina

Mrs. Rosa Maria Ríos-pelegrina

orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 April 2022 in Environmental Research
Verified
Journal Article
Open access
PSPilar Sánchez
Pilar Sánchez
BCBeatriz Castro
Beatriz Castro
SMSergio Martínez-Rodríguez
Sergio Martínez-Rodríguez
RRRosa Maria Ríos-pelegrina
Rosa Maria Ríos-pelegrina
RMRaimundo G. del Moral
Raimundo G. del Moral
EOEsperanza Ortega
Esperanza Ortega
The synergetic effect of estrogens and androgens is known to play a crucial role in the physiopathology of the prostate gland. Bisphenol A (BPA) is an endocrine disrupting compound that can interfere with endocrine hormone functioning and thereby influence prostate development. The objective of this study was to examine the impact on prostate expression of aromatase, 5α-R isozymes, and prostate cancer-related genes of exposure to low doses of BPA from perinatal period to adulthood. Vehicle or BPA (2.5 μg/kg b.w./day) was administered to gestating Wistar rats from gestational day 12 (GD12) to parturition and then to their male pups from postnatal day 1 (PND1) until euthanization on PND90. Their prostate glands were examined by qRT-PCR, Western blot, PCR array, and morphological study. mRNA and protein levels of 5α-R2 were significantly reduced and mRNA and protein levels of aromatase were significantly increased in BPA-treated animals, which also showed modifications of 8 out of the 84 key genes implicated in the development of prostate cancer. Because BPA interferes with genes involved in intraprostatic androgen and estrogen production and others implicated in prostate cancer, research is warranted into the prostate disease risk associated with chronic low-dose BPA exposure throughout life.

14 December 2017
Verified
Journal Article
Closed access
Pablo Galindo-MorenoPablo Galindo-Moreno
Pablo Galindo-Moreno
JLJesús López-Martínez
Jesús López-Martínez
MMMercedes Caba Molina
Mercedes Caba Molina
RRRosa Maria Ríos-pelegrina
Rosa Maria Ríos-pelegrina
LTLaura Torrecillas-Martínez
Laura Torrecillas-Martínez
FOFrancisco O'Valle
Francisco O'Valle

16 November 2014 in Case Reports in Medicine
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Journal Article
Open access
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RRRaquel Rios-Fernández
Raquel Rios-Fernández
JCJosé-Luis Callejas-Rubio
José-Luis Callejas-Rubio
MCMercedes Caba-Molina
Mercedes Caba-Molina
RRRosa Maria Ríos-pelegrina
Rosa Maria Ríos-pelegrina
NONorberto Ortego-Centeno
Norberto Ortego-Centeno
Mesenteric inflammatory venoocclusive disease is an uncommon cause of intestinal ischemia. Certain diseases, such as hypercoagulation disorders, autoimmune diseases, or drugs have been associated with the pathogenesis of mesenteric inflammatory venoocclusive disease. Here, we report a patient with Sjögren’s syndrome who underwent surgery for suspected acute appendicitis with a subsequent pathological diagnosis of mesenteric inflammatory venoocclusive disease.

1 June 2015 in Journal of Hand and Microsurgery
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Journal Article
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PHP. Hernández-Cortés
P. Hernández-Cortés
MCM. Caba-Molina
M. Caba-Molina
RGR. Gómez-Sánchez
R. Gómez-Sánchez
RRRosa Maria Ríos-pelegrina
Rosa Maria Ríos-pelegrina
Hand metastasis represents between 0.007 and 0.2 % of all metastatic lesions [1, 2]. Renal cell carcinoma accounts for only 10–12 % [3, 4] of these infrequent lesions. Finger metastases are commonly misdiagnosed due to their low frequency and because they can resemble an infectious condition [5]. We report a case of renal clear cell carcinoma with distal phalangeal metastasis and review the related literature. This case highlights the need to consider acrometastasis in the differential diagnosis of digital lesions in patients with renal clear cell carcinoma. A 53-year-old right-handed man was seen by his family physician for pain and swelling in right fifth finger after a minor trauma; he had a history of disseminated renal clear cell carcinoma (RCC) with radiation-resistant metastases in lung and fourth lumbar and was under combined treatment with sunitinib and everolimus. The initial diagnosis was an infection, which was unsuccessfully treated with NSAIDs, cloxa ...

15 April 2014 in Medical Principles and Practice
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Journal Article
Open access
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ARAna María Almodóvar Real
Ana María Almodóvar Real
Alejandro Molina-LeyvaAlejandro Molina-Leyva
Alejandro Molina-Leyva
MEMaría Jose Espiñeira-Carmona
María Jose Espiñeira-Carmona
RRRosa Maria Ríos-pelegrina
Rosa Maria Ríos-pelegrina
RNRamón Naranjo-Sintes
Ramón Naranjo-Sintes
HEHusein Husein El-Ahmed
Husein Husein El-Ahmed
Objective: We present a case of eosinophilic pustular folliculitis, a rare dermatosis which is often associated with HIV infection or internal malignancies. Clinical Presentation and Intervention: We report the case of a 66-year-old man with a medical history of hypertension. Histopathological examination showed a dense follicular inflammatory infiltrate with abundant eosinophils. The clinical response to indomethacin was excellent with no recurrence during the follow-up. Conclusion: The patient responded well to indomethacin treatment.

1 January 2018 in Revista Española de Enfermedades Digestivas
Verified
Journal Article
Closed access
CCCarmelo Diéguez Castillo
Carmelo Diéguez Castillo
AMAlicia Martín-Lagos Maldonado
Alicia Martín-Lagos Maldonado
RRRosa Maria Ríos-pelegrina
Rosa Maria Ríos-pelegrina
MAMaría del Mar Díaz Alcázar
María del Mar Díaz Alcázar
ACAmparo Roa Colomo
Amparo Roa Colomo
EEElena Ruiz Escolano
Elena Ruiz Escolano
Sarcoidosis is a systemic granulomatous disease with an uncertain etiology, characterized by the production of non-necrotizing granulomas. The most frequent presentation is pulmonary and mediastinal, although it might affect any other organ. Hepatic alterations occur in 50 to 65% of the cases. Nevertheless, it is commonly subclinical or detected during a study of the alteration of liver enzymes. It is very unusual that disease onset occurs as an isolated hepatic tumor. A hepatic biopsy is usually required to confirm the diagnosis. A differential diagnosis must be established via any hepatic granulomatous disease, infectious or autoimmune disease as well as the exclusion of malignancy. We present a clinical case of a female diagnosed with an isolated hepatic sarcoidosis that simulated a unique hepatic metastatic lesion.The hepatic biopsy was diagnostic.