Aneurysm of the dorsalis pedis artery: case report and literature review
(Portuguese PDF version)

Marcelo Iost Bausells1, Selma Regina de Oliveira Raymundo2, Adinaldo Adhemar Menezes da Silva3, Marcelo Rocha Casagrande1, Daniel Gustavo Miquelin1, Luiz Fernando Reis4

1. Resident doctor, Division of Vascular Surgery, Hospital de Base de São José do Rio Preto.
2. Head professor of vascular surgery, Faculdade de Medicina de São José do Rio Preto.
3. Professor of vascular surgery, Faculdade de Medicina de São José do Rio Preto.
4. Physician, Division of Vascular Surgery, Hospital de Base de São José do Rio Preto.

Correspondence:
Dr. Marcelo Iost Bausells
Rua Maranhão, 43/32
CEP: 01240-001- São Paulo - SP
Tel.: +55 (11) 3259.4441
E-mail: marcelobausells@hotmail.com


ABSTRACT

The present article reports a case of a male child with aneurysm of the dorsalis pedis artery. Diagnosis was confirmed by duplex scanning and pathoanatomical examination. End-to-end anastomosis was performed. Six months later, the lesion reappeared. A new duplex scan showed integrity of the anastomosis and revealed another aneurysm immediately close to this one. An angiographic study was performed and showed complete plantar arch. The aneurysm was resected and the dorsal foot artery was ligated. A pathological examination evidenced arterial dissection after anastomosis. During a six-month follow-up period after the second surgery, no recurrence was noted. Most of the published case reports related to pseudoaneurysms. True aneurysms are relatively rare. A discussion about the etiology, epidemiology and treatment of this type of aneurysm is also presented.

Key-words: aneurysm, artery, surgery.
Palavras-chave: aneurisma, artéria, cirurgia.

J Vasc Br 2003;2(1):26-28


INTRODUCTION

True aneurysm of the dorsalis pedis artery is a rare condition, especially among children. It is usually associated with factors such as arteriosclerosis, collagen disease and syphilis, among others. The present study describes the case of a child with aneurysm of the left dorsalis pedis artery, which had been free of disease or history of trauma. The epidemiology, etiology and surgical treatment of the aneurysm are discussed and literature reviewed.

CASE REPORT


A 4-year-old male child was assessed by our division of vascular surgery after being evaluated by pediatricians. The child presented with a pulsatile mass for approximately two years. The mass was located on the dorsal region of the left foot, next to the ankle, and was about 1 cm in diameter. It was painless, with fibroelastic consistency, and with no inflammatory signs at the site No rapid growth had been noticed in the last few months and there was no previous history of trauma or related diseases at the site. The child did not show characteristics of a syndrome.

After consultation, a duplex scan was performed, which showed aneurysmal dilation of the dorsalis pedis artery, with diameters of at most 4.9 mm x 8.9 mm, with no signs of thrombi in them. The examination of the abdominal aorta and of the iliac and visceral arteries was uneventful (Figures 1, 2, 3 and 4).

click hereFigure 1 - Preoperative duplex scanning.

click hereFigure 2 - Duplex scan after first surgery.

click hereFigure 3 - Arteriography after first surgery.

click hereFigure 4 - Intraoperative aspect.

The child was submitted to surgical treatment for aneurysm excision and end-to-end anastomosis. The pathoanatomical examination confirmed the existence of true aneurysm, which was 1.2 cm in length and 0.5 cm in diameter.

The surgical wound healed completely in the postoperative period. The control duplex scan, carried out one month after the surgery, yielded normal results.

Six months after the surgery, the pulsatile lesion reappeared under the surgical scar. A new duplex scan revealed integrity of the end-to-end anastomosis and dilation of the aneurysm after anastomosis, with a size of 6.3 mm x 8.2 mm (Figures 5 and 6). A selective arteriography of the left lower limb showed normal femoral, popliteal, and tibial arteries and dilation of the dorsalis pedis artery, which extended from the tarsus to the proximal half of the metatarsal bones. The plantar arch was unaffected, with complete filling through both tibial arteries (Figures 7 and 8).

A second surgery, which consisted of excision of the lesion and ligation of the dorsalis pedis artery, was performed (Figures 9, 10 and 11). The pathoanatomical examination showed dissecting aneurysm in the anastomosed segment of the artery.

We observed appropriate perfusion of the foot in the postoperative period. The follow-up until six months after the surgery did not show recurrence of the lesion.

DISCUSSION

Arterial aneurysms result from two basic mechanisms: (1) intrinsic, due to structural fragility of the vessel wall, and (2) due to mechanical stress of the arterial wall. Several pathological processes are associated with arterial aneurysms, among which, we have Marfan syndrome, Ehlers-Danlos syndrome, syphilis, diabetes, infections, trauma, atherosclerosis and fibrodysplasia.

The aorta is the most frequently affected artery, followed by femoral and popliteal arteries. Aneurysms are clinically characterized by a pulsatile mass, and may present or not thrill or murmur. Arteriography, computed tomography, magnetic resonance, and ultrasonography are routinely used to confirm the diagnosis, check the extension of the problem and relationships with other anatomical structures.

The aneurysms of the dorsalis pedis artery are rarely reported, but we believe they occur quite often. Of the 15 case reports found in the literature, most were concerned with pseudoaneurysms1-5 in children, usually related to trauma or orthopedic surgery.

Few of the reported cases relate to true aneurysms. Herrmann 7 described aneurysm in a 42-year-old patient and associated it with arteriosclerosis. The lesion was excised, with end-to-end anastomosis of the artery.

Wu 8 reported aneurysm of the dorsalis pedis artery in a 52-year-old male patient, who was submitted to resection of the lesion and ligation of the arterial stumps. The pathoanatomical examination revealed true aneurysm, with mural thrombus and thin arterial walls.

Fitzpatrick9 and Morettini et al. 10 reported another two cases, described as idiopathic and isolated, respectively. Both patients presented risk factors for arteriosclerosis.

McKee & Fisher6 described a case of a 71-year-old, diabetic and hypertensive woman, in whom the aneurysm was excised after ligation of the dorsalis pedis artery. The histopathological exam revealed epithelioid hemangioma.

Some studies suggest that if aneurysm is observed at this site, other sites should be inves tigated by careful clinical examination and imaging exams. Immunoelectrophoresis, anti-smooth muscle antibody and antinuclear antibody panels and serology for syphilis should be requestedm.9,10 A histopathological exam of the vessel wall and a microbiological exam of the surgical specimen are crucial for the investigation of mycotic aneurysm.

Clinical conduct, with periodical reassessments of the lesion, was adopted in some cases. Most cases required surgical intervention, which consisted of excision of the lesion followed by end-to-end anastomosis of the artery,1,2,7,10 in order to preserve vascular integrity, ensuring normal development in children and adolescents at risk of developing atherosclerosis. However, the definitive ligation of the artery is another treatment option that can be carried out safely.

In the reported case, as it involved a child, we decided for arterial repair on the first surgery, as recommended by the literature; such procedure was also adopted due to the easy approximation of the proximal and distal stumps of the artery it allows. Our decision for permanent ligation of the artery on the second surgery was rather based on technical aspects than on the possibility of recurrence of the disease, since the histopathological exam showed dissection of the arterial wall next to the anastomosis as reason for recurrence of the disease.

The imaging exams did not show other aneurysms or vascular abnormalities. The preoperative exams and the pathoanatomical exams did not detect the etiology of the disease, and the lesion was considered to be a true aneurysm of the dorsalis pedis artery, with idiopathic nature.

REFERENCES

1. Chairman EL, Uricchio JN. Traumatic aneurysm of dorsalis pedis artery: a review of the literature and case report. J Am Podiatry Assoc 1982;72:41-3.

2. Bogokowsky H, Slutzski S, Negri M, Halpern Z. Pseudoaneurysm of dorsalis pedis artery. Injury 1985;16:424-5.

3. Lieberman JR, Goldstock LE, Jacobs RL. Pseudoaneurysm of the dorsalis pedis artery after Lisfranc amputation. Foot Ankle 1991;12:123-4.

4. Vasudevan A, Patel D, Brodrick P. Pseudoaneurysm of the dorsalis pedis artery [letter]. Anaesthesia 1997;52:926-7.

5. Enzinger FM, Weiss SW. Soft tissue tumors. 2nd ed. St. Louis: CV Mosby; 1988. p. 502-8.

6. McKee TI, Fisher JB. Dorsalis pedis artery aneurysm: Case report and literature review. J Vasc Surg 2000;31:589-91.

7. Herrmann M. Pedal aneurysms [letter]. Eur J Vasc Endovasc Surg 1996;11:250.

8.Wu KK. True aneurysm of dorsalis pedis artery mimicking a soft tissue tumor. J Foot Surg 1991;30:304-7.

9. Fitzpatrick WH. Idiopathic aneurysm of the dorsalis pedis artery. J Foot Surg 1980;19:185-6.

10. Morettini G, Ventura M, Marino GA, Petrassi C, Spartera C. Isolated aneurysm of the dorsalis pedis artery. Eur J Vasc Endovasc Surg 1995;9:485-6.


J Vasc Br - Official Publication of the Brazilian Society of Angiology and Vascular Surgery