Proteus syndrome: clinical and radiological findings through a new case report

Abstract

Background

Proteus syndrome (PS) is a complex and uncommon disorder with as its main feature a patchy or mosaic postnatal overgrowth. A high clinical and radiological variability characterizes it.

Case presentation

We report the case of a 2-year-old boy presenting with lipomas and diagnosed as PS in front of general criteria (sporadic occurrence, progressive course, and mosaic distribution of lesions) and specific criteria (linear epidermal nevus in the chest and asymmetric and overgrowth in the upper limbs) of Biesecker. The course of the disease was marked by a huge overgrowth of arms despite several surgeries. By the age of 10 years, a painful swelling of the right forearm revealed a venous thrombosis on a venous malformation.

Conclusions

This case report highlights the variability of clinical findings in PS. It also emphasizes the contribution of routine imaging tools for the diagnosis and the follow-up of this rare disease.

Background

Proteus syndrome (PS) is a rare congenital syndrome that can be categorized as a hamartomatous disorder. This syndrome is characterized by a great clinical variability due to a bony and soft tissue overgrowth [1]. Diagnostic criteria for PS were controversial making difficult its diagnosis. This complex disorder is thought to affect fewer than 200 individuals in the developed world [2].

The radiologist interferes at so many levels, using practically different imaging tools in accordance with the highly variable manifestations of this disorder. The diagnosis, the follow-up, the detection of complications, and even the prenatal screening depend heavily on imaging findings [3].

We report the case of a boy diagnosed as having a PS, and we review the role of the radiologist in the multidisciplinary management of this rare pathology.

Case presentation

Our patient is the second living child of unrelated parents. He had one older healthy sister. His mother was 33 years old, and his father was 40 years old at the time of his birth. There was no significant family medical history. His examination was unremarkable at birth. An accelerated and asymmetric growth of the upper limbs from the age of 9 months was noted by parents. No diagnosis was made at this age. At 2 years and half, he was investigated for subcutaneous masses in the upper right limb. The diagnosis of lipomas was retained on biopsy and the child was referred to the pediatrics department.

The diagnosis of PS was taken into consideration based on Biesecker criteria 2006 (Table 1) [4]. These criteria were the most recent at the time of the first patient’s consultation in 2008.

Table 1 Revised diagnostic criteria for proteus syndrome (Biesecker 2006)

The diagnosis of PS was retained on the proband based on the presence of all general criteria (sporadic occurrence, progressive course of the disease, mosaic distribution of lesions) and two specific criteria from category B (linear epidermal nevus in the upper chest, asymmetric and disproportionate overgrowth of upper limbs). Besides, he had macrodactyly and syndactyly in the left hand. Genetic screening was not done in our patient because it was not affordable.

The boy was referred to the orthopedic department. He was operated on three times to help stop the overgrowing of arms and fingers bones. The last surgery was made at 6 years old. He was then lost to follow-up due to the family’s financial difficulties. He was readmitted to the pediatrics department at 10 years old for an inflammatory swelling in the right forearm. We noticed an important overgrowth of his arms and fingers (Fig. 1), a scoliosis, an overgrowth of adenoids, and a hepatomegaly (liver span at 11 cm). His psychomotor development was normal.

Fig. 1

Disproportionate overgrowth of the left arm and hand associated with syndactyly (A). Chest epidermal nevi and soft tissue hypertrophy (B)

X-ray assessment revealed multiple skeletal anomalies (Fig. 2, Fig. 3).

Fig. 2

X-ray of the left hand (G) showing disproportional overgrowth of the fingers, phalangeal and metacarpal demineralization, and degenerative deformities along with soft tissue overgrowth

Fig. 3

X-rays of left arm (G) and right arm(D) demonstrating elbows and fingers deformities and soft tissue overgrowth

The abdominal ultrasound exam was normal except for hepatomegaly.

Right forearm’s ultrasound exam coupled with Doppler showed “low-flow” tortuous “polycystic and communicating lesions with no apparent flow-signal at rest (Fig. 4, Fig. 5). If repeatedly compressed by the HR-US probe, the lesions appeared soft and well compressible and showed a typical color-shift signal within. The above-mentioned features were related to venous malformations. A dilated vein was filled with echogenic material and was not compressible corresponding to a thrombotic vein (venous malformation affected by thrombophlebitis) (Fig. 6).

Fig. 4

B-mode ultrasonography of the right forearm: multiple cystic communicating lacunae

Fig. 5

Color Doppler ultrasonography of the right forearm: low-flow” tortuous “polycystic and communicating vessels on corresponding to capillary and venous malformations

Fig. 6

Doppler ultrasonography of the right forearm: Dilated, not compressible vein filled with echogenic material without flow signal corresponding to the thrombotic vein

The patient was put on low molecular weight heparin with favorable outcome.

The subsequent course was marked by several episodes of thrombosis of the superficial veins in upper limbs with favorable outcome under medical treatment. The patient has never had a pulmonary embolism with a follow-up of 8 years (Fig. 7).

Fig. 7

Timeline of the case report

Discussion

Mosaic overgrowth syndromes are a group of uncommon diseases presenting as asymmetric, segmental, and often progressive overgrowth involving any tissue type. Clinical presentations are discordant ranging from isolated malformations to life-threatening conditions. These syndromes result from mosaic somatic, post-zygotic mutations in genes involved in cell growth and proliferation. The PI3K/AKT/mTOR signaling pathway is mainly involved. Proteus syndrome is an AKT1-related syndrome [5].

PS was rarely reported in Tunisian children. This syndrome remains little-known in our country, and our case report emphasizes an illustrative phenotype. In addition, our case is not limited to the clinical presentation but specifies the radiological particularities, a key point in the diagnosis and management of this syndrome. Our main limitation is the absence of a genetic study, but this does not hinder the diagnosis.

Proteus syndrome (OMIM # 176,920) is a rare overgrowth condition. It was first described in 1979, by Hayden and Cohen, in two patients [1]. It is a highly polymorph and complex disease that associates overgrowth of multiple tissues and malformations. No two patients with PS are exactly alike. Most of the affected persons appear healthy at birth, but typically during the child’s first year, some parts of their bodies begin to grow faster and larger than they should [6].

Diagnosis of PS is challenging and evolving. Its intrinsic variability made it necessary to establish diagnostic criteria in 1999 [7]. These criteria were revised in 2006 [4].

A mosaic activating AKT1 mutation (c.49G > A, p.Glu17Lys) was identified in PS. This was first published in 2011 [8].

Biesecker et al. in a study published in 2019 presented a new approach to diagnose PS. Most of the diagnosis criteria were used unmodified (Biesecker, 2006; Biesecker et al., 1999). However, other factors were added. It was about pulmonary embolism, vein thrombosis, and other tumor types testicular cystadenomas/adenocarcinomas and meningiomas. Cardiac septal lipoma was also added in the category “lipomas/dysregulated adipose. Finally, the authors added two negative criteria: substantial prenatal extracranial overgrowth and ballooning overgrowth since uncommon in PS. Subsequently, they set a boundary at ≥ 15 points to consider an individual to have a clinical diagnosis of PS in the absence of an AKT1 variant. Individuals with a score of ≥ 10 points and a pathogenic mosaic variant in AKT1 were considered as having AKT1-related PS. In the case of a score of 2 to 9 points associated with pathogenic mosaic variant in AKT1, the diagnosis of AKT1-related overgrowth spectrum was retained [9]. The diagnosis of PS was retained in our patient in 2008 based on the Biesecker et al. 2006 criteria [4]. This diagnosis was reassessed according to Biesecker et al. 2019 criteria [9]. According to this new approach, our patient has a score of 16 (all general criteria; asymmetric, disproportionate overgrowth of limbs, and scoliosis (5 points); overgrowth of adenoids and liver (5 points); lipomas (2 points); linear epidermal nevus (2 points); and venous malformations (2 points)). Screening for AKT1 mutation has not been done due to financial considerations. Although we have no genetic confirmation for PS, this diagnosis was retained since we have a score of 16. Other syndromes partially superimposable to PS such as CLOVES syndrome, neurofibromatosis 1, or PTEN hamartoma tumor [10] were excluded based on clinical, histological, and radiological presentation in our patient.

PS is also characterized by orthopedic complications which are one of the most challenging medical problems. Various cutaneous and subcutaneous lesions (lipomas, vascular malformations and several types of nevi) are also evocative. Most commonly vascular malformations are of capillary type. However, some patients have venous malformations. Arterial vascular malformations are uncommon in PS. Intracranial arteriovenous malformations were described in one case [6, 7].

The typical ultrasound aspect of venous malformation is a polycystic, sponge-like, pseudo-tumorous lesion positioned subcutaneously and composed of complex and communicating venous vessels [2, 11]. The separating walls may be of variable thickness which renders the B-mode appearance very inhomogeneous. Thrombotic precipitates filling the vascular lumen are sometimes found. They are due to vascular wall abnormalities and to very low blood flow velocities. Indeed, patients with PS are at risk to get deep vein thrombosis, which can lead to pulmonary embolism [12]. Males appear to be at greater risk for thrombosis than females. It is important for doctors caring for people with PS to be aware of this risk [13]. Our patient presented a thrombosis 8 years after initial diagnosis.

Accurate management of patients with PS can be very well assessed through several imaging modalities.

Multiple imaging techniques are useful in the evaluation of PS. A radiograph skeletal survey is needed to identify bone anomalies. CT of the chest is helpful in the evaluation for pulmonary embolism. Abdominal and pelvic CT or MRI can be used to evaluate visceromegaly and to search for asymptomatic but potentially aggressive lipomatosis. Central nervous system MRI is needed to identify brain anomalies in patients with neurologic symptoms [2, 11].

Ultrasonography is very useful to characterize the subcutaneous lesions. Besides, it offers, with the use of the Doppler, the possibility to assess vascular malformations and to easily diagnose venous thrombosis. The latter occurs at an increased frequency in PS and exposed to pulmonary embolism major cause of premature death.

The 2004 guidelines indicate for patient assessment [2]:

• –Serial clinical photography

• –Initial skeletal survey with targeted follow-up radiographs

• –MR imaging of clinically affected areas and in asymptomatic patient, an MRI of chest and abdomen

• –Dermatologic and orthopedic consultations as long with a pediatric management

Radiologic findings are multiple. Table 2 summarizes the most common ones in patient with PS [2]. The current treatment of PS is mainly symptomatic and aims to decrease disability and promote a better quality of life. AKT1 inhibitor miransertib seems to be an interesting molecule to investigate [13].

Table 2 Radiologic findings in Proteus syndrome

Conclusion

Proteus syndrome is a rare pathology involving a variety of organs and thus implicating different physicians. The high variability of clinical presentation makes the diagnosis challenging. The management depends on the results of the first assessment based on physical examination and imaging investigation. Being aware of the radiological specificities of PS is essential for diagnosis and follow-up. To increase the accuracy of diagnosis, the use of the most recent published diagnostic is recommended. However, radiological assessment is particularly useful in low-income countries where genetic testing is not usually affordable as in our patients.