Abstract
The coracobrachialis muscle (CBM) originates from the apex of the coracoid process, in common with the short head of the biceps brachii muscle, and from the intermuscular septum. Both the proximal and distal attachment of the CBM, as well as its relationship with the musculocutaneus nerve demonstrate morphological variability, some of which can lead to many diseases. The present case study presents a new description of a complex origin type (four-headed CBM), as well as the fusion of both the short biceps brachii head, brachialis muscle and medial head of the triceps brachii. In addition, the first and second heads formed a tunnel for the musculocutaneus and median nerves. This case report has clear clinical value due to the split mature of the coracoid process, and is a significant indicator of the development of interest in this overlooked muscle.
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Introduction
The flexor compartment of the arm contains the biceps brachii, brachialis and coracobrachialis (CBM) muscles. The CBM originates from the apex of the coracoid process, in common with the short head of the biceps brachii muscle (BBM), and from the intermuscular septum. It inserts by means of a flat tendon into an impression at the middle of the medial surface and border of the body of the humerus, between the origins of the triceps brachii and brachialis muscles [32]. The CBM is innervated by the musculocutaneous nerve (MCN) [32].
The role of the CBM is twofold: it flexes and adducts the arm at the glenohumeral joint, and prevents the arm from being deviated from the frontal plane during abduction. Therefore, during contraction, the CBM causes shoulder flexion by drawing the humerus forward, and shoulder adduction by drawing it toward the torso. It also turns the humerus slightly inwards, thus causing internal rotation. The CBM also stabilizes the humeral head within the shoulder joint, especially when the arm hangs freely [32].
Many earlier works describe the various types of morphological variations occurring within this muscle. Some relate to accessory slips of the muscle inserting to the medial epicondyle and medial supracondylar ridge of the humerus, medial intermuscular septum of the arm, others examine additional heads or bellies, while others relate to morphological variations in the proximal or distal attachment [3, 15,16,17, 21, 25, 31]. Morphological variations between CBM and MCN have also been noted, namely the nerve does not pierce the muscle [10, 11, 15, 25, 47].
The presence of additional bellies for the CBM may cause musculocutaneous or high median nerve paralysis [15, 25].
This study describes a very rare case of CBM, i.e. a quadrifurcated form with a tunnel for the median nerve and MCN; it can hence act as a potential compression site for these nerves. Knowledge of such a rare type can make it easier to understand disease entities in this region and improve their treatment.
Case report
Morphology of the coracobrachialis muscle
A 71-year-old female cadaver was subjected to routine anatomical dissection for research and teaching purposes in the Department of Anatomical Dissection and Donation, Medical University of Lodz, Poland. A traditional anatomical dissection of the right upper limb was performed [35,36,37,38, 41], during which, the CBM was found to be quadrifurcated—Figs. 1, 2, 3 and 4.
The next stage of the procedure involved a detailed assessment of the CBM. The CBM was characterized by four independent proximal attachments which connect with each other in the distal part; the muscle is inserted by means of a flat tendon into an impression at the middle of the medial surface and border of the humerus body. The distal part of one of the bellies was fused with the brachialis muscle—Fig. 3.
The first two heads of the CBM demonstrate a proximal attachment at the “accessory apex” of the coracoid process of the scapula—Figs. 1, 2, 5, 6 and 7. The first, i.e. more superficial, head displaying attachments to the “accessory apex” of the coracoid process of the scapula was 77.60 mm long while the second (deeper) head, located on the inferior surface of the “accessory apex” was 71.02 mm in length. These heads closely resemble the standard attachment of this muscle; however, in this case, they represent a unilateral muscle and both the MCN and median nerve pass between the two heads—Fig. 8. The two bellies connect with each other and pass into the tendon which is 71.72 mm long—Figs. 1 and 2.
The third head, together with the head of the short biceps brachii, was attached to the apex of the coracoid process and was characterized by a fusion with the head of the short biceps brachii—Figs. 1 and 2. The length of the third head was 113.51 mm and was attached to the tendons of the first and second heads of the CBM. The fourth head was the longest (155.11 mm); it was located under the head of the short biceps brachii and displayed an attachment at the inferior surface of the coracoid process. In the distal part, it demonstrated a fusion to the brachialis muscle, with the distal attachment being at the middle of the medial surface and the border of the body of the humerus, together with the other three heads—Figs. 1 and 2.
The four heads of the CBM were innervated by the MCN—Figs. 4 and 8.
Detailed morphometric measurements were then taken. After photographic documentation, the CBM was carefully dissected to minimize any errors in measurement. The measurements were performed using two methods.
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By electronic calliper (Mitutoyo Corporation, Kawasaki-shi, Kanagawa, Japan). Each measurement was carried out twice with an accuracy of up to 0.1 mm.
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Analysis of digital photographic images processed through MultiScanBase 18.03 (Computer Scanning System II, Warsaw, Poland).
Accurate morphometric measurements can be found in Table 1.
The relation of the nerves to the coracobrachialis muscle
Both MCN and the lateral root of the median nerve ran between the first and second CBM heads (muscle belly part). The mean width of the MCN passage is 3.60 mm, and that of the lateral root median nerve is 4.25 mm. The median nerve then passes between the second and third head to the anterior part of the arm; its mean width here is 4.28 mm—Fig. 8.
Anatomical variations of the coracoid process of the scapula
The coracoid process of the scapula was characterized by a split, with two apexes visible—Figs. 1, 2, 4, 5, 6 and 7. The proximal attachments of the first and second head of the CBM had on the accessory apex, while the third and fourth heads of the CBM and the short head of the biceps brachii had the origin on the apex of the coracoid process (Table 2).
Discussion
The coracobrachialis muscle (CBM) has greater morphological than functional significance. It is, morphologically, the sole representative of the adductor group in the arm, but this functionality has been lost phylogenetically over time. The CBM has three distinct parts in amphibians, reptiles, and monotremes:
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(1)
the coracobrachialis brevis, inserting into the humerus, superior to the latissimus dorsi tendon,
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(2)
the coracobrachialis medius, inserted into the humerus, inferior to latissimus dorsi tendon,
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(3)
the coracobrachialis longus or Wood’s muscle; this extends inferiorly on the shaft of humerus, where it bridges the median nerve and brachial artery.
In some primates, the CBM is composed of two parts, which is roughly equivalent to the coracobrachialis brevis. In man, it is formed of a single part; this may derive from the coracobrachialis medius of the lower animals, or from the fusion of the two heads observed in apes and prosimians; in the latter case, the MCN would be trapped between them [19, 51].
Embryologically, the variants of the CBM are believed to derive from the lateral mesoderm, together with the other muscles of the upper limb. The muscle primordia are believed to fuse to form a single body which regresses as the layers of the muscles develop. The presence of an accessory CBM could be explained as a results of the premature termination of this regression [11, 17]. The split in the scapula may arise from (a) the displacement of one of the ossification centers in utero or (b) the existence of more than two ossification centers; in this case, one of them forms a supernumerary clavicle [30, 46]. In mammals, the shoulder girdle is usually ossified from two centers, resulting in the formulation of the scapula and the coracoid process. In this case, it is possible that the ossification center for the coracoid process was single in the early period of development; it later formed a broad base that split into two from the center [30, 46].
Although the muscle commonly demonstrates morphological variations in proximal or distal attachment as well as in relation to MCN, not so much variation is observed regarding the occurrence of additional heads or bellies [8, 10, 11, 16, 17, 21, 51].
The original third head of the CBM, i.e. the coracobrachialis brevis, originates from the coracoid process and inserts into the crest of the lesser tubercle or the intertubercular groove and to the articular capsule of the shoulder joint; however, this variation is rarely seen [3,4,5, 8, 25, 28, 49]. The coracobrachialis brevis has also been found to attach to the shoulder joint capsule or the surgical neck of the humerus; the coracobrachialis longus might also attach to the humerus, to a fibrous band of the medial intramuscular septum, i.e. Struther’s ligament, or to the medial epicondyle [6, 50, 51]; it may also attach to the tendinous part of the latissimus dorsi [6, 51]. The CBM has been found to connect to the brachialis muscle [50], or to the brachial fascia [21]. A fetal study identified an insertion to the brachial fascia [25].
In our present study, a connection was observed between the fourth head of the CBM and the brachialis muscle (Fig. 1). A previous study described a CBM with three portions originating from the coronoid process of the scapula and inserting into the medial epicondyle of the humerus (longus), humeral diaphysis (medius) and to the humeral neck (brevis) [28]. Elsewhere another CBM variant demonstrated two bellies which formed shortly inferior to its origin from the coracoid process of the scapula: one belly inserted into the middle of the antero-medial surface of the humerus, while the other inserted into the medial head of the triceps brachii muscle [12].
Our present findings indicate the presence of a “fascial–tendinous” combination between the first, second and the third head of the CBM, and the medial head of the triceps brachii. Elsewhere, distal muscle insertions have been observed in the middle of the anteromedial humerus surface, forming an aponeurotic arch shape expansion fixed in the lateral epicondyle [11]. A three-headed CBM has also been reported previously; the first head originated from the superior border of the scapula over the scapular notch and inserted into the upper third of the medial part of the medial intramuscular septum, the second corresponded to the classical description of the CBM. Finally, the third head demonstrated proximal and distal tendinous portions and an intermediate muscle belly, the proximal tendinous part originated from the coracoid process, and inserted to the medial epicondyle of the humerus [16].
CBMs were found to be divided into superficial and deep layers in 16% of a Japanese population and incompletely divided in 8% [33]. This resembles the present case, where three of the four heads are superficial, while the fourth head is located deep under the short head of the biceps brachii. The first, second, third heads in the distal part connect to each other and attach between the brachialis muscle and the medial head of the triceps brachii. The positioning of the fourth head of CBM is very interesting. It was located under the head of the short biceps brachii and attached to the inferior surface of the apex of coracoid process; its distal part also demonstrated a fusion to the brachialis muscle, and the distal attachment was at the middle of the medial surface and border of the humerus body, together with the other three heads of CBM.
Can this fourth head represent the third head of the biceps brachii? Various types of attachment have been described for the third head of the biceps brachii, including the humeral shaft, short head of the biceps brachii and the pectoralis major [1, 26, 27]. Regarding attachment sites, in the present case, the proximal attachment was located on the scapula and the distal attachment at a site typical for CBM insertion; therefore, it appears that the fourth head is not the third head of the biceps brachii.
The CBM is believed to be functionally unimportant; however, some studies suggest that it is one of the most effective flexors of the shoulder joint and that it also resists anterior dislocation [2]. The CBM connects to the short head of the biceps brachii, and to the brachialis muscle (they are the flexors), demonstrating that it supports the pair of them. It is very interesting that the combination of three heads connects superficially with the medial head of the triceps brachii, which suggests that this structure may assist the medial head of the triceps brachii, which is an extensor; this is really interesting, because presented CBM attaches to the muscles that have an antagonistic function.
The frequency of the atypical course and relation of the MCN to CBM has been exhaustively described in the literature [10, 11, 14, 21, 29, 45, 48]. The MCN innervates the CBM in 0–22% of cases [11, 12, 14, 21, 29, 45].
A variable relationship with the surrounding nerves was observed in the present case. Both the musculoskeletal nerve and the lateral median nerve root ran between the first and second CBM heads. However, a previous studies have found the extra head of the CBM to form a “tunnel” for the median nerve and brachial artery [11] and an accessory head of the CBM which involved the lateral cord of the brachial plexus [15].
Both the CBM and accessory CBM, as well as the accessory heads of the muscle are of significant clinical importance. The CBM could be used as a guide to the axillary artery during surgery and anesthesia, and its distal attachment marks the site of the nutritional artery of the humerus [52]. The accessory head of the CBM is also of special interest in that traction on an osteomized coracoid might be expected to jeopardize not only the MCN but also a portion of the median nerve [14, 25].
The additional head identified in the present study also places pressure on both the MCN and MN, as the latter also wraps distally around the CBM. In this case, if pressure occurs, both the anterior compartment of the arm and the forearm muscle may be affected. For this reason, consideration should be given to the accessory head of the muscle before performing coracoid mobilization. MCN lesion can occur during coracoid bone block abutment (Bristow–Latarjet). The muscle inserting to the coracoid process needs to be mobilized and retracted when performing coracoid abutment transfer by Latarjet via the deltopectoral approach. This can lead to injury to the MCN, a known complication of procedures concerning the anterior shoulder. Transient lesion of the MCN may also occur following its elongation and the modification of its angle of penetration into the muscle [9]. A split coracoid process can also hinder transfer by Latarjet. In addition, other possible variations in this area should be taken into account.
Therefore, it would be advisable to perform MRI and CT of the area before planned procedures, as they play a significant role in the evaluation of anatomical and pathological lesions and anatomical variations of the shoulder and upper limb.
To summarise, surgery or interventional radiology in the shoulder and arm area should be preceded by thorough diagnostic tests to assess the presence of additional bellies or heads of the CBM. In addition, the exact course of both the MCN and MN should be assessed, together with the posterior cord to the CBM.
Morphological variations of the scapula are also quite common. These usually apply to the acromion, glenoid process and subscapular notch [20, 23, 34, 39, 40, 42,43,44]. In contrast, no morphological variability of the coracoid process has been observed so far; most studies concern morphometric measurements [18, 22, 24].
The present case report describes the first occurrence of a split coracoid process connected with four-headed CBM. A thorough understanding of the normal anatomy and morphological variation occurring within the acromion, coracoid process and related structures with the glenohumeral joint is necessary to correctly interpret radiological images or plan surgical procedures in the shoulder area. To avoid injury to vital neurovascular structures medial to the coracoid process, such as the brachial plexus and axillary vessels, most shoulder procedures are based on a lateral approach to the coracoid process [7, 13]. Knowledge of the anatomical variations of the coracoid process of the scapula and morphometric measurements is, therefore, highly relevant in surgical procedures involving the shoulder joint, such as hardware fixation, drill hole placement and prosthetic positioning.
Conclusion
The CBM is characterized by great morphological variability and a variable relationship with the MCN and MN. Knowledge of these variations is necessary when planning surgical procedures in the shoulder and shoulder area, and appropriate diagnostic tests should be performed to identify additional CBM muscle heads. Knowledge of the anatomical variations of the coracoid process of the scapula and morphometric measurements is, therefore, highly relevant in surgical procedures. The presented rare case combined aforementioned muscular and bone variations and describes the first occurrence of a split coracoid process together with four-headed coracobrachialis muscle.
Data availability
Please contact authors for data requests (Łukasz Olewnik PhD—email address: lukasz.olewnik@umed.lodz.pl).
References
Asvat R, Candler P, Sarmiento EE (1993) High incidence of the third head of biceps brachii in South African populations. J Anat 182(Pt 1):101–104
Bassett RW, Browne AO, Morrey BF, An KN (1990) Glenohumeral muscle force and moment mechanics in a position of shoulder instability. J Biomech 23:2–3. https://doi.org/10.1016/0021-9290(90)90295-E
Bauones S, Moraux A (2015) The accessory coracobrachialis muscle: ultrasound and MR features. Skeletal Radiol 44:1273–1278. https://doi.org/10.1007/s00256-015-2153-1
Beattie PH (1947) Description of bilateral coracobrachialis brevis muscle, with a note on its significance. Anat Rec 97:123–126
Bechtol CO (1954) Coracobrachialis brevis. Clin Orthop 4:152 (Cited in: Warner JP, Paletta GA, Warren RF (1992) Accessory head of the biceps brachii.Clin Orthop 280: 179–181)
Bergman R, Afifi A, Miyauchi R (2017) Illustrated encyclopedia of human anatomic variations. Anatomy atlas: Opus I: muscular system: alphabetical listing of muscles. https://www.anatomyatlases.org/AnatomicVariants/MuscularSystem/Text/P/29Plantaris.shtml. Accessed 14 Apr 2020
Bhatia DN, De Beer JF, Du Toit DF (2007) Coracoid process anatomy: implications in radiographic imaging and surgery. ClinAnat 20:774–784. https://doi.org/10.1002/ca.20525
Chouke K (1924) Variation of the coracobrachialis muscle. Anat Rec 1:157–161
Clavert P, Lutz JC, Wolfram-Gabel R, Kempf JF, Kahn JL (2009) Relationships of the musculocutaneous nerve and the coracobrachialis during coracoid abutment procedure (Latarjet procedure). SurgRadiolAnat 31:49–53. https://doi.org/10.1007/s00276-008-0426-2
El-Naggar MM (2001) A study on the morphology of the coracobrachialis muscle and its relationship with the musculocutaneous nerve. Folia Morphol (Warsz) 60:217–224
El-Naggar MM, Al-Saggaf S (2004) Variant of the coracobrachialis muscle with a tunnel for the median nerve and brachial artery. ClinAnat 17:139–143. https://doi.org/10.1002/ca.10213
El-Naggar MM, Zahir FI (2001) Two bellies of the coracobrachialis muscle associated with a third head of the biceps brachii muscle. ClinAnat 14:379–382. https://doi.org/10.1002/ca.1067
Feng D, Zhang X, Jiang Y, Zhu Y, Wang H, Wu S, Zhang K, Wang Z, Zhang J (2018) Plate fixation through an anterior approach for coronoid process fractures: a retrospective case series and a literature review. Med (US) 97:1–12. https://doi.org/10.1097/MD.0000000000012041
Flatow EL, Bigliani LU, April EW (1989) An anatomic study of the musculocutaneous nerve and its relationship to the coracoid process. ClinOrthopRelat Res. https://doi.org/10.1097/00003086-198907000-00014
Garbelotti SA, Marques SR, Rocha PR, Pereira VR, De Moraes LOC (2017) An unusual case of accessory head of coracobrachialis muscle involving lateral cord of brachial plexus and its clinical significance. Folia Morphol 76:762–765. https://doi.org/10.5603/FM.a2017.0033
Georgiev GP, Landzhov B, Tubbs RS (2017) A novel type of coracobrachialis muscle variation and a proposed new classification. Cureus 9:1–6. https://doi.org/10.7759/cureus.1466
Georgiev GP, Tubbs RS, Landzhov B (2018) Coracobrachialislongus muscle: humeroepitrochlearis. Cureus 10:5–9. https://doi.org/10.7759/cureus.2615
Gregori M, Eichelberger L, Gahleitner C, Hajdu S, Pretterklieber M (2020) Relationship between the Thickness of the coracoid process and Latarjet Graft positioning—an anatomical study on 70 embalmed scapulae. J Clin Med 9:207. https://doi.org/10.3390/jcm9010207
Guha R, Satyanarayana N, Reddy C, Jayasri N, Nitin V, Praveen G, Sunitha P, Datta A (1970) Variant insertion of coracobrachialis muscle-morphological significance, embryological basis and clinical importance. J Coll Med Sci 6:42–46. https://doi.org/10.3126/jcmsn.v6i2.3616
Guo X, Ou M, Yi G, Qin B, Wang G, Fu S, Zhang L (2018) Correction between the morphology of acromion and acromial angle in Chinese population: a study on 292 scapulas. Biomed Res Int 2018:1–13. https://doi.org/10.1155/2018/3125715
Ilayperuma I, Nanayakkara BG, Hasan R, Uluwitiya SM, Palahepitiya KN (2016) Coracobrachialis muscle: morphology, morphometry and gender differences. SurgRadiolAnat 38:335–340. https://doi.org/10.1007/s00276-015-1564-y
Jen CL, Toon DH, Tan CH (2020) Radiological study of the Asian coracoid process and clavicle: implications for coracoclavicular ligament reconstruction. Chin J Traumatol English Ed 23:56–59. https://doi.org/10.1016/j.cjtee.2019.05.007
Jezierski H, Podgórski M, Wysiadecki G, Olewnik Ł, De Caro R, Macchi V, Polguj M (2018) Morphological aspects in ultrasound visualisation of the suprascapular Notch region: a study based on a new four-step protocol. J Clin Med 7:491. https://doi.org/10.3390/jcm7120491
Jia Y, He N, Liu J, Zhang G, Zhou J, Wu D, Wei B, Yun X (2020) Morphometric analysis of the coracoid process and glenoid width: a 3D-CT study. J OrthopSurg Res 15:3–4. https://doi.org/10.1186/s13018-020-01600-1
Kopuz C, Içten N, Yildirim M (2003) A rare accessory coracobrachialis muscle: a review of the literature. SurgRadiolAnat 24:406–410. https://doi.org/10.1007/s00276-002-0079-5
Kosugi K, Shibata S, Yamashita H (1992) Supernumerary head of biceps brachii and branching pattern of the musculocutaneus nerve in Japanese. SurgRadiolAnat 14:175–185. https://doi.org/10.1007/BF01794898
Kumar H, Das S, Rath G (2008) An anatomical insight into the third head of biceps brachii muscle. Bratislava Med J 109:76–78
Kyou-Jouffroy MK, Lessertisseur J, Saban R, Souteyrand-Boulenger JD (1971) Musculature des membres, membre pectoral, groupe branchial ventral. In: Traité de zoologie, mammifères, vol XVI, part III. Masson, Paris, pp 96–98
Loukas M, Aqueelah H (2005) Musculocutaneous and median nerve connections within, proximal and distal to the coracobrachialis muscle. Folia Morphol (Warsz) 64:101–108
McBain L, Simonds E, Iwanaga J, Tubbs RS (2018) Review of the pathology and congenital anomalies of the coracoid process with clinical applications. Transl Res Anat 10:4–6. https://doi.org/10.1016/j.tria.2017.12.001
Mestdagh H, Maynou C, Cassagnaud X (2002) Accessory coracobrachialis muscle as a cause of anterior impingement syndrome of the rotator cuff in an athlete. Eur J OrthopSurgTraumatol 12:96–98. https://doi.org/10.1007/s00590-002-0021-x
Moore K, Dalley A (2006) Lower limb. Clinically oriented anatomy. Wilkins, Lippincott Williams and Wilkins, Philadelphia
Mori M (1964) Statistics on the musculature of the Japanese. Okajimas Fol Anat Jpn 40:195–300. https://doi.org/10.2535/ofaj1936.40.3_195
Nayak G, Panda SK, Chinara PK (2020) Acromion, coracoid and glenoid processes of scapula: an anatomical study. Int J Res Med Sci 8:570. https://doi.org/10.18203/2320-6012.ijrms20200237
Olewnik Ł, Podgórski M, Polguj M, Wysiadecki G, Topol M (2018) Anatomical variations of the pronator teres muscle in a Central European population and its clinical significance. AnatSciInt 93:299–306. https://doi.org/10.1007/s12565-017-0413-y
Olewnik Ł, Waśniewska A, Polguj M, Podgórski M, Łabętowicz P, Ruzik K, Topol M (2018) Morphological variability of the palmarislongus muscle in human fetuses. SurgRadiolAnat 40:1283–1291. https://doi.org/10.1007/s00276-018-2069-2
Olewnik Ł, Wysiadecki G, Polguj M, Podgórski M, Jezierski H, Topol M (2017) Anatomical variations of the palmarislongus muscle including its relation to the median nerve—a proposal for a new classification. BMC MusculoskeletDisord 18:1–9. https://doi.org/10.1186/s12891-017-1901-x
Podgórski M, Olewnik Ł, Rusinek M, Cichosz M, Polguj M, Topol M (2019) 'Superior biceps aponeurosis’—morphological characteristics of the origin of the short head of the biceps brachii muscle. Ann Anat 223:85–89. https://doi.org/10.1016/j.aanat.2019.01.014
Podgórski M, Topol M, Sibiński M, Domzalski M, Grzelak P, Polguj M (2015) What is the function of the anterior coracoscapular ligament? A morphological study on the newest potential risk factor for suprascapular nerve entrapment. Ann Anat 201:38–42. https://doi.org/10.1016/j.aanat.2015.06.005
Podgórski M, Topol M, Sibiński M, Grzelak P, Stefańczyk L, Polguj M (2014) New parameters describing morphological variations in the suprascapular notch region as potential predictors of suprascapular nerve entrapment. BMC MusculoskeletDisord 15:11–12. https://doi.org/10.1186/1471-2474-15-396
Podgórski MT, Olewnik Ł, Grzelak P, Polguj M, Topol M (2019) Rotator cable in pathological shoulders: comparison with normal anatomy in a cadaveric study. AnatSciInt 94:53–57. https://doi.org/10.1007/s12565-018-0447-9
Polguj M, Jedrzejewski K, Podgórski M, Majos A, Topol M (2013) A proposal for classification of the superior transverse scapular ligament: Variable morphology and its potential influence on suprascapular nerve entrapment. J Shoulder ElbSurg 22:1265–1273. https://doi.org/10.1016/j.jse.2012.11.017
Polguj M, Sibiński M, Grzegorzewski A, Grzelak P, Majos A, Topol M (2013) Variation in morphology of suprascapular notch as a factor of suprascapular nerve entrapment. IntOrthop 37:2185–2192. https://doi.org/10.1007/s00264-013-2005-3
Polguj M, Synder M, Kwapisz A, Stefańczyk K, Grzelak P, Podgõrski M, Topol M (2015) Clinical evaluation of the shape of the suprascapular notch—an ultrasonographic and computed tomography comparative study: application to shoulder pain syndromes. ClinAnat 28:774–779. https://doi.org/10.1002/ca.22582
Remerand F, Laulan J, Couvret C, Palud M, Baud A, Velut S, Laffon M, Fusciardi J (2010) Is the musculocutaneous nerve really in the coracobrachialis muscle when performing an axillary block? An ultrasound study. AnesthAnalg 110:1729–1734. https://doi.org/10.1213/ANE.0b013e3181dc25c8
Sharma BG (2003) Duplication of the clavicle with triplication of the coracoid process. Skeletal Radiol 32:661–664. https://doi.org/10.1007/s00256-003-0696-z
Tatar I, Brohi R, Sen F, Tonak A, Celik H (2004) Innervation of the coracobrachialis muscle by a branch from the lateral root of the median nerve. Folia Morphol (Warsz) 63:503–506
Venieratos D, Anagnostopoulou S (1998) Classification of communications between the musculocutaneous and median nerves. ClinAnat 11:327–331. https://doi.org/10.1002/(SICI)1098-2353(1998)11:5<327:AID-CA6>3.0.CO;2-M
Warner J, Paletta G, Warren RF (1992) Accessory head of the biceps brachii. ClinOrthopRelat Res 1:179–181
Wood J (1864) On some varieties in human myology. Proc R Soc Lond 13:299–303
Wood J (1867) On human muscular variations and their relation to comperative anatomy. J AnatPhysiol 1:44–59
Woodworth GE, Katz J (1992) Thecoracobrachialis muscle: a guide to the axillary artery. RegAnesth 17:180–181. https://doi.org/10.1136/rapm-00115550-199217030-00015
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ŁO (D.P.T., PhD)—associate professor—project development, data collection and management, data analysis and manuscript writing. NZ—student—data analysis, manuscript editing. PK—assistant—data analysis, manuscript editing. FD (MD., PhD)—professor—data analysis, manuscript editing. GPG (MD., PhD)—Assist. Prof—data analysis and manuscript editing. MP (MD., PhD)—professor—data analysis, manuscript editing. All authors have read and approved the manuscript.
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Olewnik, Ł., Zielinska, N., Karauda, P. et al. The co-occurrence of a four-headed coracobrachialis muscle, split coracoid process and tunnel for the median and musculocutaneous nerves: the potential clinical relevance of a very rare variation. Surg Radiol Anat 43, 661–669 (2021). https://doi.org/10.1007/s00276-020-02580-x
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DOI: https://doi.org/10.1007/s00276-020-02580-x