{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T10:15:52Z","timestamp":1785406552358,"version":"3.56.0"},"reference-count":8,"publisher":"Universidad Nacional de C\u00f3rdoba","issue":"1","license":[{"start":{"date-parts":[[2026,3,13]],"date-time":"2026-03-13T00:00:00Z","timestamp":1773360000000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc\/4.0"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Rev Fac Cien Med Univ Nac Cordoba"],"abstract":"<jats:p>Objectives: Describe the clinical case of a RICH that was diagnosed in uterus, normally in obstetric ultrasounds they are often confused with arteriovenous malformations and other congenital tumors. The differential diagnosis of these entities is important, since they have a different evolution, prognosis and treatment.\r\nClinical case: The clinical case of a RICH with incipient signs of heart failure is presented, it required an interdisciplinary approach with dermatologists, neonatologists, obstetricians and specialists in diagnostic imaging, to define diagnosis, conduct and follow-up. Postnatal follow-up was performed until complete and spontaneous involution, leaving almost no sequelae, despite the large size of the tumor.\r\nConclusion: It is important to take into consideration the diagnosis of RICH, among intrauterine high-flow vascular tumors, so as not to perform unnecessary interventions.<\/jats:p>","DOI":"10.31053\/1853.0605.v83.n1.44679","type":"journal-article","created":{"date-parts":[[2026,3,30]],"date-time":"2026-03-30T17:04:41Z","timestamp":1774890281000},"page":"e44679","source":"Crossref","is-referenced-by-count":0,"title":["Hemangioma cong\u00e9nito r\u00e1pidamente involutivo, diagnosticado prenatalmente con insuficiencia card\u00edaca y seguimiento postnatal"],"prefix":"10.31053","volume":"83","author":[{"given":"Agustina","family":"Santarelli","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/04qtr9c10","id-type":"ROR","asserted-by":"publisher"}],"name":"Hospital Privado"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mar\u00eda Candelaria","family":"Gimenez","sequence":"additional","affiliation":[{"name":"Hospital Infantil de C\u00f3rdoba"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mar\u00eda Dolores","family":"Salduna","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/04qtr9c10","id-type":"ROR","asserted-by":"publisher"}],"name":"Hospital Privado"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Enrique","family":"Valente","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/04qtr9c10","id-type":"ROR","asserted-by":"publisher"}],"name":"Hospital Privado"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"12333","published-online":{"date-parts":[[2026,3,13]]},"reference":[{"key":"ref0","doi-asserted-by":"crossref","unstructured":"1. Larralde M, Sol\u00e9 JJ, Luna PC, Mosquera T, Abad ME. Hemangiomas cong\u00e9nitos r\u00e1pidamente involutivos: serie de 25 casos [Rapidly involuting congenital hemangiomas: twenty five case series]. Arch Argent Pediatr. 2014 Apr;112(2):e61-5. Spanish. doi: 10.5546\/aap.2014.e61. DOI: 10.5546\/aap.2014.e61 DOI: 10.5546\/aap.2014.e61","DOI":"10.5546\/aap.2014.e61"},{"key":"ref1","unstructured":"2. Panizzard, AA. Hemangiomas cong\u00e9nitos. secci\u00f3n 17.2.2. p\u00e1g 454-455. En: Larralde M, Abad ME, Luna P. Dermatolog\u00eda Pedi\u00e1trica, 3ra ed. Buenos Aires, Argentina: Ediciones Journals, 2021."},{"key":"ref2","unstructured":"3. Frieden IJ, Adams DM. Congenital hemangiomas: Rapidly involuting congenital hemangioma (RICH), noninvoluting congenital hemangioma (NICH), and partially involuting congenital hemangioma (PICH). Feb 2024, UpToDate."},{"key":"ref3","doi-asserted-by":"crossref","unstructured":"4. Sur A, Manraj H, Lavoie PM, Lim K, Courtemanche D, Brooks P, Albersheim S. Multiple Successful Angioembolizations for Refractory Cardiac Failure in a Preterm with Rapidly Involuting Congenital Hemangioma. AJP Rep. 2016 Mar;6(1):e99-e103. doi: 10.1055\/s-0035-1570342. DOI: 10.1055\/s-0035-1570342 DOI: 10.1055\/s-0035-1570342","DOI":"10.1055\/s-0035-1570342"},{"key":"ref4","doi-asserted-by":"crossref","unstructured":"5. Fadell MF 2nd, Jones BV, Adams DM. Prenatal diagnosis and postnatal follow-up of rapidly involuting congenital hemangioma (RICH). Pediatr Radiol. 2011 Aug;41(8):1057-60. doi: 10.1007\/s00247-010-1967-1. DOI: 10.1007\/s00247-010-1967-1 DOI: 10.1007\/s00247-010-1967-1","DOI":"10.1007\/s00247-010-1967-1"},{"key":"ref5","doi-asserted-by":"crossref","unstructured":"6. Chen CP, Chen CY, Chang TY, Yang HY, Chen YN, Chen SW, Wang W. Prenatal imaging findings of a rapidly involuting congenital hemangioma (RICH) over right flank in a fetus with a favorable outcome. Taiwan J Obstet Gynecol. 2016 Oct;55(5):745-747. doi: 10.1016\/j.tjog.2016.07.008. DOI: 10.1016\/j.tjog.2016.07.008 DOI: 10.1016\/j.tjog.2016.07.008","DOI":"10.1016\/j.tjog.2016.07.008"},{"key":"ref6","unstructured":"7. Fa\u00fandez E, Schrag B, Ram\u00edrez C, Mor\u00e1n M. Hemangioma cong\u00e9nito r\u00e1pidamente involutivo, RICH. Rev Chilena Dermatol. 2011; 27(1):86-93."},{"key":"ref7","doi-asserted-by":"crossref","unstructured":"8. Weitz NA, Lauren CT, Starc TJ, Kandel JJ, Bateman DA, Morel KD, Meyers PM, Kadenhe-Chiweshe A, Wu JK, Garzon MC. Congenital cutaneous hemangioma causing cardiac failure: a case report and review of the literature. Pediatr Dermatol. 2013 Nov-Dec;30(6):e180-90. doi: 10.1111\/j.1525-1470.2012.01875.x. 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