[Bilateral congenital triangular alopecia associated with congenital heart disease and renal and genital abnormalities].
نویسندگان
چکیده
MT, San Juan J, López D, Carda C. Matrical carcinoma with prominent melanocytic hyperplasia (malignant melanocytic matricoma?). A report of two cases. Am J Dermatopathol. 2003; 25:485-9. 9. Rizzardi C, Melato M. Simply, the point is that pathologists should bear in mind melanocytic matricoma. Am J Dermatopathol. 2003;25:447. 10. Resnik KS. Isn’t melanocytic matricoma simply one expected histopathologic expression of matricoma? Am J Dermatopathol. 2003;25:446. 11. Resnik KS. Is melanocytic matricoma a bona fide entity or is it just one type of matricoma? Am J Dermatopathol. 2003;25:166. 12. Rizzardi C, Melato M. Is melanocytic matricoma a bona fide entity or is it just one type of matricoma?: splitting hairs... in hair matrix tumors! Author’s reply. Am J Dermatopathol. 2003;25: 166-7. 13. Carlson JA, Slominski A, Mihm MC Jr. What are the clinicopathologic features of matricoma? Am J Dermatopathol. 2003;25:446-7. 14. Monteagudo Sánchez B, Pereiro Ferreirós M. Paciente con varios tumores en los antebrazos. Piel. 2004; 19:51-2. 15. Monteagudo Sánchez B, León Muiños E, Durana C, Cacharrón Carreira JM, de las Heras Sotos C. Pilomatricoma anetodérmico. An Pediatr (Barc). 2006; 64:181-2. 16. Izquierdo MJ, Requena C, Requena L. Pilomatricoma. En: Neoplasias anexiales cutáneas. Madrid: Grupo Aula Médica; 2004. p. 309-17. 17. Spitz D, Fisher D, Friedman RJ, Kopf AW. Pigmented pilomatricoma. A clinical simulator of malignant melanoma. J Dermatol Surg Oncol. 1981;7: 903-6. 18. Zaim MT. Pilomatricoma with melanocytic hiperplasia: an uncommon occurrence and a diagnostic pitfall. Arch Dermatol. 1971;104:117-23. 19. Cazers JS, Okun MR, Pearson H. Pigmented calcifying epithelioma. Review and presentation of a case with unusual features. Arch Dermatol. 1974; 110: 773-4. LETTERS TO THE EDITOR
منابع مشابه
Coagulation Abnormalities in Pediatric Patients with Congenital Heart Disease: A Literature Review
It has been recognized that patients with Cyanotic Congenital Heart Disease (CCHD) show significant bleeding tendency which can be secondary to coagulopathies in these patients. Some coagulation abnormalities are thrombocytopenia, factor deficiencies, fibrinolysis and Disseminated Intravascular Coagulation (DIC). According to high prevalence of CCHD and major operations in theses patients, th...
متن کاملسندرم نونان (گزارش یک مورد)
Noonan syndrome is a genetic condition inherited by an autosomally dominant manner, characterised by congenital heart disease, short stature, abnormal facies and the somatic feature of Turner's syndrome, but a normal karyotype. Noonan syndrome affects approximately 1 in 1500 live births. Congenital heart disease occurs in 35-50% of patients diagnosed with noonan syndrome. The most common cardia...
متن کاملHematologic Abnormalities in Cyanotic Congenital Heart Disease Patients
Introduction:Patients with cyanotic heart disease may have an acceptable quality of life. However, they are invariably prone to several complications. The aim of this study is search about hematologic abnormalities in cyanotic congenital heart disease patients. Materials and Methods: In this cross sectional study every cyanotic congenital heart disease patients who was referred to the adult co...
متن کاملبررسی فراوانی ناهنجاری های مادرزادی آشکار و عوامل همراه آن در نوزادان بستری در بخش نوزادان بیمارستان های فاطمیه و بعثت همدان در سال 1394
Background & Aims: Congenital anomaly is characterized by any anatomical defects present in a baby at birth that may cause major medical, surgical, or cosmetic consequences. the present study aimed to determine the prevalence of congenital anomalies and related factors among infants in Hamadan Fatemiyeh and Behesht hospitals in 2015. Materials & Methods: this case series study...
متن کاملEvaluating the overt extracardiac malformations in children with congenital heart disease in Khuzestan Province
Background: Extracardiac malformations can be seen in 20-45% of infants with congenital heart disease (CHD). Chromosomal abnormalities exist in 5-10% of patients with CHD. The aim of this study was to assess the frequency of overt extra cardiac malformations in children with CHD. Methods: This descriptive epidemiologic study was conducted on 720 patients with CHD referred to the pediatric ca...
متن کاملHolt-Oram Syndrome: A Rare Variant
Holt-Oram syndrome is an autosomal dominant disorder, characterised by skeletal abnormalities of the upper limb associated with congenital heart defect, mainly atrial and ventricular septal defects. Skeletal defects exclusively affect the upper limbs in the preaxial radial ray distribution and are bilateral and asymmetrical. They range from clinodactyly, absent or digitalised thumb, hypoplastic...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Actas dermo-sifiliograficas
دوره 99 7 شماره
صفحات -
تاریخ انتشار 2008