The lateral portion of the flexor plate of the leg gives rise to GM and SM, while the PM arises proximally to the SM and on the GM tibial side [3]. The superficial muscles of the posterior leg compartment (GM, SM, PM) are not well differentiated before the 2nd developmental month. These muscles’ variants seem to occur due to separation problems of the original anlage into the three independent muscles (GM, SM, PM). The GM supernumerary head (3rd head) may be defined as a congenital muscle mass (or tendinous head), usually originating from the distal dorsal surface of the femur that joins the LH, MH, or both heads of GM [4].

The most investigated variant of the GM, due to its clinical significance, is the presence of a third head, the so-called “GT”. In the current case, a bilateral presence of a three-headed GM was identified. Bergman et al. [2] noted a prevalence of the GT, ranging between 2.9 and 5.5%. Koplas et al. [5] in their imaging study of 1,039 magnetic resonance images (MRI), identified a GT in 2% of their sample. In all cases, the 3rd head originated from the posterior distal femur and fused with the LH, while it coursed laterally to the popliteal vessels. Only a unique case of a bilateral appearance of a GT was identified [5]. The bilateral GT has been reported in the case studies of Arefi et al. [6], Ishii et al. [7], and Yildirim et al. [8]. Arefi et al. [6] reported a similar case to the present one, while Ishii et al. [7] reported a quite smaller Gand hypoplastic GT (morphologically similar to the PM). Yildirim et al. [8] identified the coexistence of a bilateral GT with an accessory SM, similar to the coexistence of the GT with a unilateral two-headed PM, in the present case. Hence, the GT occurrence is considered relatively uncommon (2-5.5%), while its bilateral presence is considered even rarer and has been reported in only four published cases [5-8]. Except for the three-headed GM, there are extremely rare cases of quadriceps GM, as Koplas et al. [5] identified in a unique case of their sample (<0.01%).

Recently, the PM has gained a lot of clinical interest due to its value for the tendons’ reconstruction in the hand and lateral ankle ligament reconstruction [1]. In the current report, a two-headed PM was identified with a distinct insertion medially to the calcaneal tendon. Olewnik et al. [9] in their morphological study of the PM in 142 adult lower limbs, classified the muscle’s morphology into six types. Type I corresponded to the typical presentation of the muscle (48.4%), while in type II, the PM originated partially from the GM LH and partially from the knee joint capsule (25%). Type III was characterized by an origin from the lateral femoral condyle and the knee joint capsule (10.15%), while in type IV, the origin was from the lateral femoral condyle, the knee joint condyle, and the iliotibial band (6.25%). Type V PM originated only from the lateral femoral condyle (8.6%) and type VI included “rare cases” (1.6%). Type VI was further divided into type VIa (0.8%), which included a double PM with two distinct muscular and two tendinous parts, and type VIb (0.8%), which included a PM with two distinct muscular parts forming a single tendon. The present described PM morphological variant corresponded to Olewnik Type VIb (0.8%), a similar finding to Smędra et al. [10] who reported a unilateral PM with two heads that fused into a common tendon. Olewnik et al. [11] and Maślanka et al. [12] identified three-headed PMs. Except from its origin, Gonera et al. [1] in their systematic review of PM morphology created a classification system for its insertion. Gonera type I PM insertion refers to the calcaneal tuberosity with a course medial to the calcaneal tendon with an estimated prevalence between 24-48%. In the current case, the PM insertion corresponds to the Gonera type I.

Implications may manifest concerning the presentation of a third-headed GM, mainly involving compression of the popliteal neurovascular bundle. PA entrapment and/or PV, and/or TN was first described by Hamming (1959) due to the appearance of a muscular congenital anomaly, the abnormal 3rd head of GM (as cited by Connell [13]). The third head may or may not cross the popliteal neurovascular bundle or some portion of the neurovascular bundle before insertion into GM or its tendon [4]. Koplas et al. [5] and Arefi et al. [6] pointed out the compression effect of the various components of the popliteal neurovascular bundle, presenting with the symptomatology of nerve entrapment, such as tibial or sciatic neuropathy. In cases of GM aberrant heads and their neural supply (TN thin branches), the available space in the popliteal fossa is decreased between adjacent structures, and vascular entrapment neuropathy of the TN may occur within the GM. Such chronic cases of neuropathy may also present with GM atrophy [14]. Differential diagnosis of entrapment neuropathy or vasculopathy cases includes a range of conditions, such as intraneural ganglion cyst affecting the sciatic nerve lower divisions, adventitial cyst in the PA, thrombophlebitic syndrome due to lower extremity deep vein thrombosis, synovial sarcoma in the knee joint, popliteal entrapment syndrome, posterior compartment syndrome in the lower leg, PA aneurysm, and Baker cyst [5, 6, 15]. It is important also to consider the GT variants among these clinical entities. In addition, PM variants have been implicated in Achilles tendon tendinopathy; hence, in recurrent cases, PM variants should also be considered [1]. Meticulous clinical examination and further imaging are essential for establishing the diagnosis.

In the current case, a bilateral three-headed GM coexisted with a unilateral two-headed PM. These two variants, independently, are considered rare, while their coexistence has not been reported. Especially, the GT variant could potentially cause compression to popliteal neurovascular structures. The coexistence of these variants should alert clinicians, to avoid pitfalls and iatrogenic lesions.