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Copyright of Acta Pediatrica de Mexico is the property of Instituto Nacional de Pediatria (INP) and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Background: The newborn congenital epulis or granular cell tumor is a benign tumor that appears in the oral cavity of newborns with more frequency in the gingiva of the alveolar crest of the maxilla at the level of the incisive and canine area, predominantly in the female sex. It is of diagnostic importance since it can interfere with feeding, swallowing and via area, putting the health of the newborn at risk. It usually involutes spontaneously and in case of surgical treatment there are no reports of recurrence. The aim of this work was to describe the evolution according to the approach of this patient with congenital newborn epulis. Case report: The case of a patient of the newborn congenital epulis and its follow-up for 6 years is reviewed. Conclusions: The surgical treatment of the newborn congenital epulis seems to be a good option of approach without the difficulties in the feeding, suction and breathing of the newborn. [ABSTRACT FROM AUTHOR]

Copyright of Acta Pediatrica de Mexico is the property of Instituto Nacional de Pediatria (INP) and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Acta Pediatrica de Mexico is the property of Instituto Nacional de Pediatria (INP) and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Chronic mucocutaneous candidiasis is characterized by infections caused by Candida sp, usually Candida albicans, which may be persistent or recurrent on skin, mucous membranes and nails; generally confined on the cutaneous surface and occasionally systemic dissemination. This can be associated to endocrinopathies and autoimmunity. We report a case of chronic mucocutaneous candidiasis with thyroid disease resilient to itraconazole with positive response to voriconazole and immunostimulation. [ABSTRACT FROM AUTHOR]

Atopic dermatitis is a chronic inflammatory disorder of the skin occurs during the first years of life affecting about 10 to 20% of children. It is often associated with allergy problems and usually responds to topical or systemic antihistamines, but there are cases resistant to treatment. We report a case of severe recalcitrant atopic dermatitis unresponsive to conventional treatments with response to treatment with omalizumab. [ABSTRACT FROM AUTHOR]

Aldrich syndrome (WAS) is an X-linked primary immunodeficiency, associated with WASP gene mutation that causes severe immunological abnormalities and alterations in platelet function. A seven year old male patient with WASP, began with acute abdominal pain, fever and knee swelling. The diagnosis of septic arthritis was made, and he was treated with broad-spectrum antibiotics and human gammaglobulin. During treatment he presented digestive tract bleeding with hypovolemic shock; after 72 hours palpable purpura in upper and lower extremities appeared. Then Henoch-Schönlein purpura with abdominal vasculitis was suspected, and later confirmed by histopathology. Methylprednisolone pulses were initiated, showing improvement within 24 hours. The patient had a severe inflammatory reaction, caused by a serious infectious disease, but the clinical evolution suggested an autoimmune disease such as Henoch-Schönlein purpura. Up to 20% of patients with WAS have autoimmune manifestations of vasculitis. An early diagnosis of autoimmunity in WAS is important for a favorable clinical outcome. [ABSTRACT FROM AUTHOR]