Hemolacria. Reality or fiction?

Authors

  • Jairo Jesus Gomez Tejeda Universidad de Ciencias Medicas de Holguin
  • Aida Elizabeth Iparraguirre Tamayo Universidad de Ciencias Médicas de Cuba
  • Odalis Tamayo Velázquez Policlinico Docente de Gibara José Martí

Keywords:

hemolacria, hemolacrimia, blood tears

Abstract

Introduction: hemolacria is a rare phenomenon of tears that are completely or partially composed of blood. Currently, one case is reported for every one million inhabitants, and their predilection towards a specific gender, race or age is unknown. Objective: to describe the causative agents of hemolacria as a nosological entity. Material and Method: abibliographic review was made based on a total of 29 bibliographic references used. Articles from national and international journals from the databases, Medline, Scielo, Elsevier and Open Journal were used. Articles were selected that had a maximum of 5 years or less of having been published. The quality, reliability and validity of the selected articles were analyzed for an adequate review. Development: hemolacria is a physical condition, which causes the production of tears that are completely or partially composed of blood. It can manifest itself as tears that contain some reddish tones until they appear to be made entirely of blood. Among the causes are conditions of the ocular structures, hereditary hemorrhagic telangestacia, congenital deficiency of coagulation factor VII, hypertension, some benign neoplasms, acute myeloid leukemia and excessive use of drugs such as warfarin.Conclusions: hemolacria is a symptom of numerous diseases and is caused by various ocular, systemic, psychological, pharmacological and idiopathic conditions.

Author Biographies

Jairo Jesus Gomez Tejeda, Universidad de Ciencias Medicas de Holguin

Estudiante

Odalis Tamayo Velázquez, Policlinico Docente de Gibara José Martí

Especialista en primer grado de MGI y Medicina Interna. Profesor asistente.

References

1. Jakobiec F, Wolkow N, Zakka F, Rubin P. Myeloid Sarcoma with Megakaryoblastic Differentiation Arising in the Conjunctiva. Ocul Oncol Pathol [Internet]. 2019 [citado 2019 Ene 10]; 5: 28-35. Disponible en: https://10.1159/000488057

2. Di Maria A, Famà F. Hemolacria- Sangre Que Llora. N Engl J Med [Internet]. 2018 [citado 2019 Ene 12]; 379: 1766. Disponible en: https://10.1056/NEJMicm1805241

3. Khanna R, et al. Hemolacria que revela un melanoma primario del conducto nasolagrimal. CAN J OPHTHALMOL [Internet]. 2018 [citado 2019 Ene 15]; 3(1): 201. Disponible en: https://doi.org/10.1016/j.jcjo.2018.05.009

4. Mohammad A, J, et al. Dacrioendoscopia en un caso de hemolacria inexplicable. Ophthalmic Plastic & Reconstructive Surgery [Internet]. 2018 [citado 2019 Ene 12]; 34(6):213. Disponible en: https://10.1097/IOP.0000000000001154

5. Audelan T, Best AL, Ameline V. Hemolacria: reporte de un caso clínico pediátrico. J Fr Ophtalmol [Internet]. 2019 [citado 2019 Ene 12]; 42(1):15-17. Disponible en: https://10.1016/j.jfo.2018.03.027

6. Manzano G, Shantharam R, Webb E, Finelt N, Hengel K. Case 2: Hemolacria, Hematochezia, and Hematuria in an 11-month-old Boy. Pediatr Rev[Internet]. 2018 [citado 2019 Ene 15]; 39(8):418-420. Disponible en: https://10.1542/pir.2016-0155.

7. James R, Bharadhi M, James J. Haemolacria in a 22-year-old boy. BMJ Case Reports CP [Internet]. 2018 [citado 2019 Ene 15]; 11:151-225.Disponible en: http://dx.doi.org/10.1136/bcr-2018-225151

8. Ramachandra M, Manolis H. Haemolacria a rare complication of Lefort I surgery. British Journal of Oral and Maxillofacial Surgery [Internet]. 2017 [citado 2019 Ene 12]; 55 (10): 171. Disponible en: https://doi.org/10.1016/j.bjoms.2017.08.246

9. RAHMAN MS. Trastornos disociativos con hemolacria: serie de informes de casos. J Bangladesh Coll Phys Surg [Internet]. 2017 [citado 2019 Ene 13]; 35: 36-42. Disponible en: https://www.banglajol.info/index.php/JBCPS/article/view/32571

10. Bakhurji S. A healthy infant with bloody tears: Case report and mini-review of the literatura. Saudi Journal of Ophthalmology [Internet]. 2018 [citado 2019 Ene 10]; 32 (3): 246-249. Disponible en: https://doi.org/10.1016/j.sjopt.2017.10.006

11. Gouveia, C., Evangelista, V., Almeida, R., & Baptista, A. Immune Thrombocytopenia Associated with Mycoplasma pneumoniae Infection. European Journal of Case Reports in Internal Medicine [Internet]. 2018 [citado 2019 Ene 15]; 5 (3). Disponible en: https://doi.org/https://doi.org/10.12890/2018_00081

12. Rodriguez ME, Courtney Y. K, Heather D. Potter HD. A Conjunctival Melanoma Causing Bloody Tears . Ophthal Plast Reconstr Surg [Internet]. 2017 [citado 2019 Ene 12]; 33 (3): 77. Disponible en: https://10.1097/IOP.0000000000000765

13. Mehmet P; Kadir K; Hakan D.Bilateral Idiopathic Haemolacria in a 14 Years Old Girl. Glokom-Katarakt/Journal of Glaucoma-Cataract [Internet]. 2016 [citado 2019 Ene 16]; 11 (1): 61-63. Disponible en: https://web.b.ebscohost.com/abstract

14. Sobol EK.; Barmettler A. A Case of Idiopathic Bilateral Hemolacria in an 11-Year-Old Girl. Ophthalmic Plastic and Reconstructive Surgery [Internet]. 2017 [citado 2019 Ene 12]; 33 (4): 98–99. Disponible en: https://10.1097/IOP.0000000000000811

15. Restrepo Jiménez P, Ocampo MI, Castañeda-Cardona C, Rosselli D. Síndrome de Achenbach: presentación de un caso y revisión sistemática de la literatura. Revista Colombiana de Reumatología [Internet]. 2017 [citado 2019 Ene 10]; 24 (4): 230-236. Disponible en: https://doi.org/10.1016/j.rcreue.2018.04.003

16. Block, M. E., Sitenga, J. L., Lehrer, M. and Silberstein, P. T., Gardner‐Diamond syndrome: a systematic review of treatment options for a rare psychodermatological disorder. Int J Dermatol [Internet]. 2019 [citado 2019 Ene 12]. Disponible en: https://doi.org/10.1111/ijd.14235

17. Gupta P, Di Meglio L, Behrens A. Bloody tears: a case of bilateral ulcerative blepharitis. ASIAN JOURNAL OF OPHTHALMOLOGY [Internet]. 2018 [citado 2019 Ene 9]; 16 (2). Disponible desde: https://www.asianjo.com/index.php/AsianJO/article/view/376

18. Acosta Torres J, Consuegra Otero A, Rivera Keeling C, Rodríguez Gómez O. Un caso pediátrico de hemolacria. Rev Cubana Pediatr [Internet]. 2018 [citado 2018 Nov 21]; 90 (1): 132-140. Disponible en: http://scielo.sld.cu/scielo.php?script=sci_arttext&pid=S0034-75312018000100012&lng=es

19. Franco de Acha CM, Luis Moisés Silva Goytia LM. Hemolacria bilateral con probable Telangiectasia Hemorrágica Hereditaria. Reporte de caso. Vis. Pan-Am [Internet]. 2017 [citado 2018 Jul 21]; 16 (3): 86-89. Disponible desde: https://doi.org/10.15234/vpa.v1i3.386

20. Oyenusi E, Ananti C. Haemolacria (bloodytears): A perplexingsymptom: A report of two cases. NigerianJournal of Paediatrics [Internet]. 2015 [citado 2018 Jul 23]; 42 (1): 68-70. Disponible en: https://www.ajol.info/index.php/njp/article/view/110294

21. Ullah A, Badshah M, Jamil U. Anunusual case of bloodytears. Ann IndianAcadNeurol [Internet]. 2015 [citado 2018 Jul 24]; 18 (3): 351-2. Disponible en: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4564476/

22. Mansour F, Karadsheh M. BloodyTears: A RarePresentation of MunchausenSyndrome Case Report and Review. J FamilyMed Prim Care [Internet]. 2015 [citado 2018 Jul 30]; 4 (1): 132-4. Disponible en: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4366986/

23. Eneh AA, Farmer J, Kratky V. Primarylocalized orbital amyloid: case report and literaturereview; 2004-2015. Canadian Journal of Ophthalmology [Internet]. 2016 [citado 2018 Jul 23]; 71 (4): 131-6. Disponible en: https://www.ncbi.nlm.nih.gov/pubmed/27521683

24. Eneh AA, Farmer J, Kratky V. Primarylocalized orbital amyloid: case report and literaturereview; 2004-2015. Canadian Journal of Ophthalmology [Internet]. 2016 [citado 2018 Jul 23]; 71 (4): 131-6. Disponible en: https://www.ncbi.nlm.nih.gov/pubmed/27521683

25. Vilela P, Mazza A, Chaumeil P, Miller A, Benavides O. Absceso cerebral en paciente con síndrome de Rendu-Osler-Weber. Rev de la Fac de Cienc Méd. 2016 [citado 5 Abr 2017]; 6 (4). Disponible en: http://revista.med.unlp.edu.ar/archivos/201609/absceso-cerebral-en-paciente-con-s%C3%ADndrome-de-rendu-osler-weber.pdf

26. Bustamante F, Tenreiro Picón O, Tenreiro A, Bustamante E. Síndrome de Rendu-Osler-Weber: presentación de un caso clínico. Avan Biomed. 2016 [citado 5 Abr 2017]; 5 (2). Disponible en: http://www.redalyc.org/pdf/3313/33134741700 9.pdf

27. González Escudero Mabel, Sosa Estébanez Marilyn, Pérez Acosta Noel David. Telangiectasia hemorrágica hereditaria en una gestante. MEDISAN [Internet]. 2018 [citado 2019 Nov 10] ; 22 (1): 65-70. Disponible en: http://scielo.sld.cu/scielo.php?script=sci_arttext&pid=S1029-30192018000100009&lng=es

28. Suárez Pozo R, Jiménez Delgado M, Sangroni Viart T, González Lazo J, Massuet Benítez JL, García García D. Síndrome de Gardner-Diamond. Presentación de un caso. revmedicaelectronica [Internet]. 2019 [citado 2019 Nov 10]; 41 (4): [aprox. 3 p.]. Disponible en: http://www.revmedicaelectronica.sld.cu/index.php/rme/article/view/3281

29. Pujari A, Bajaj MS. Idiopathic bilateral haemolacria. BMJ Case Rep [Internet] 2016 [citado 2018 Jul 26]. Disponible en: https://www.ncbi.nlm.nih.gov/pubmed/28039350

Published

2021-03-15

How to Cite

1.
Gomez Tejeda JJ, Iparraguirre Tamayo AE, Tamayo Velázquez O. Hemolacria. Reality or fiction?. Rev 16 de abril [Internet]. 2021 Mar. 15 [cited 2024 Dec. 12];60(279):e852. Available from: https://rev16deabril.sld.cu/index.php/16_04/article/view/852

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Review Articles

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