Clitoral erection

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Image left: Mild sexual arousal. Image right: Strong sexual arousal with erection of the vestibular bulbs under the skin on both sides of the vaginal opening and exposed clitoral glans.
3D image of a clitoris in an erect state (with the adjacent organs of the uterus and urinary bladder)

Clitoral erection is a physiological phenomenon where the clitoris becomes enlarged and firm.

Clitoral erection is the result of a complex interaction of psychological, neural, vascular, and endocrine factors, and is usually, though not exclusively, associated with sexual arousal. Erections should eventually subside, and the prolonged state of clitoral erection even while not aroused is a condition that could become painful.[1] This swelling and shrinking to a relaxed state seems linked to nitric oxide's effects on tissues in the clitoris, similar to its role in penile erection.[2]


The internal anatomy of the human vulva, with the clitoral hood and labia minora indicated as lines.

The clitoris is the homologue of the penis in the female. Similarly, the clitoris and the erection of it can subtly differ in size.[3]

The visible part of the clitoris, the glans clitoridis, varies in size from a few millimeters to one centimeter and is located at the front junction of the labia minora (inner lips), above the opening of the urethra. It is covered by the clitoral hood.

Any type of motion can increase blood flow to this organ and this results in increased secretions which lubricate the vagina. There are many ways to stimulate the clitoris.

Clitoral erection occurs when the corpora cavernosa, two expandable erectile structures, become engorged with blood. This may result from any of various physiological stimuli, including sexual arousal. During sexual arousal, arterial blood flow to the clitoris is increased, and trabecular smooth muscle within the clitoris relaxes allowing blood to engorge the erectile tissues. The ischiocavernosus and bulbospongiosus muscles contract to compress the dorsal vein of the clitoris to stop drainage of the clitoris, trapping the blood. More specifically, the clitoris has two adjoining erectile tissues corpus cavernosa (corpus cavernosa clitoridis) that form a main body that connects to the glans clitoridis. There is also a strip of erectile tissue (similar to the placement of the corpus spongiosum in males) running along the ventral surface of the corpus cavernosa main body that connects the glans clitoridis to the commissure of the vestibular bulbs.[4][5] The main body of the corpus cavernosa with a ventral erectile tissue strip make up the shaft, which is connected to the glans clitoridis. The tunica albuginea is a fibrous-elastic sheath, surrounds the shaft and glans clitoridis. The tunica albuginea does not surround the bulbs of vestibule.[6] The erectile tissues are composed of endothelium-lined vascular spaces in a trabecular matrix, with the endothelium-lined vascular spaces surrounded by smooth muscle capable of contraction and relaxation.

During sexual arousal, arterial blood flow to the clitoris is increased, and within the clitoris, the arteries further branch to supply the erectile tissues. The trabecular smooth muscles of the erectile tissue relax increasing blood flow to fill the vascular spaces, expanding the erectile tissues until they are fully engorged with blood.[4] The ischiocavernosus and bulbocavernosus muscles contract, compressing the dorsal vein of the clitoris. This compression of the vein restricts drainage of the erectile structures, trapping the blood.[7] This process stretches the tunica albuginea. As a result, the clitoris becomes tumescent to accommodate the increased intracavernosus pressure. The tunica albuginea of the clitoris is made up of one layer making it more elastic than the tunica albuginea of the penis, which is composed of two layers.[8] Erick Janssen (2007) elaborates on this reporting that "the corpora cavernosa of the clitoris are essentially similar to that of the penis except that there is no subalbugineal layer interposed between the tunica albuginea and the erectile tissue. In the penis, this[9] tissue engorges with blood during sexual arousal and becomes compressed against the unyielding tunica, creating penile rigidity --a true erection. The lack of this plexus in the clitoris indicates that while the organ can become tumescent or engorged, it cannot, like the penis, become stiffly erect. The clitoris thus does not really become erect with sexual excitement, but engorged."[9] In addition, the tunica albuginea around the glans is thinner than around the shaft in both the clitoris and penis. This gives the glans less firmness relative to the shaft. The extrusion of the glans clitoridis and thinning of the skin enhances sensitivity to physical contact. After a female has orgasmed, the erection usually ends, but this may take time.

Medical Conditions[edit]

Clitoral priapism[edit]

Priapism, while more common in males, is a condition that can also effect the clitoris.[1] Symptoms include painful engorgement of the clitoris, swelling of the clitoris, and pain in the area around the clitoris.[10]

In non-human animals[edit]

Among capuchin monkeys, clitoral erection is possible and makes the clitoris more visible than in its relaxed state where it is hidden by a preputial fold.[11]

See also[edit]


  1. ^ a b Medina, Carlos A (1 November 2002). "Clitoral priapism: a rare condition presenting as a cause of vulvar pain". Obstetrics & Gynecology. 100 (5, Part 2): 1089–1091. doi:10.1016/S0029-7844(02)02084-7. ISSN 0029-7844. PMID 12423816. S2CID 20764733.
  2. ^ Gragasin, F. S., Michelakis, E. D., Hogan, A., Moudgil, R., Hashimoto, K., Wu, X., ... & Archer, S. L. (2004). The neurovascular mechanism of clitoral erection: Nitric oxide and cGMP‐stimulated activation of BKCa channels. The FASEB journal, 18(12), 1382-1391.
  3. ^ Jackson, Lindsey A.; Hare, Adam M.; Carrick, Kelley S.; Ramirez, Denise M. O.; Hamner, Jennifer J.; Corton, Marlene M. (1 November 2019). "Anatomy, histology, and nerve density of clitoris and associated structures: clinical applications to vulvar surgery". American Journal of Obstetrics and Gynecology. 221 (5): 519.e1–519.e9. doi:10.1016/j.ajog.2019.06.048. ISSN 0002-9378. PMID 31254525. S2CID 195758555.
  4. ^ a b Bono, Christopher M.; Lin, Vernon W. (14 May 2014). Spinal Cord Medicine: Principles and Practice (2nd ed.). Demos Medical Publishing. p. 1176. ISBN 9781935281771. Retrieved 17 March 2015.
  5. ^ Clemente, Carmine D. (2010). Clemente's Anatomy Dissector. Lippincott Williams & Wilkins. p. 205. ISBN 978-1-60831-384-6. Retrieved 15 March 2015.
  6. ^ Mulhall, John P.; Incrocci, Luca; Goldstein, Irwin; Rosen, Ray (23 April 2011). Cancer and Sexual Health. Springer Science & Business Media. p. 17. ISBN 9781607619161.
  7. ^ Hornstein, Theresa; Schwerin, Jeri (1 January 2012). Biology Of Women (5th ed.). Cengage Learning. pp. 62–63 of 816. ISBN 9781285401027. Retrieved 17 March 2015.
  8. ^ Goldstein, Irwin; Meston, Cindy M.; Davis, Susan; Traish, Abdulmaged (17 November 2005). Women's Sexual Function and Dysfunction:Study, Diagnosis, and Treatment. CRC Press. p. 176. ISBN 9781842142639.
  9. ^ a b Jansen, Erick (27 September 2007). The Psychophysiology of Sex. Indiana University Press. p. 41. ISBN 9780253117045. Retrieved 29 March 2015.
  10. ^ Yafi, Faysal A.; April, Daniel; Powers, Mary K.; Sangkum, Premsant; Hellstrom, Wayne J. G. (July 2015). "Penile Priapism, Clitoral Priapism, and Persistent Genital Arousal Disorder: A Contemporary Review". Sexual Medicine Reviews. 3 (3): 145–159. doi:10.1002/smrj.51. ISSN 2050-0521. PMID 27784607.
  11. ^ Carosi, M, Spani, F, Ulland, AE, Scalici, M, Suomi, SJ. Clitoral length in immature and mature captive tufted capuchin (Sapajus spp.) females: A cross-sectional study. Am J Primatol. 2020; 82:e23135.