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Table 3 Clinical and pathological features of all known cases of AS-GCT

From: Primary pure angiosarcoma of the testis: a vanishingly rare malignancy. Case report and literature review

Case

Age (years)

Diagnosis

Presentation

Testicular lesion

 

Symptoms (duration)

Bloods

Diagnosis

Site

Size (mm)

Definitive treatment (margins)

Local recurrence

Primary angiosarcoma in germ cell tumour

MalagĂ³n et al. [15]

25

AS-GCT

N/A

N/A

Teratoma, yolk sac tumour, angiosarcoma

N/A

N/A

Orchidectomy (N/A)

N/A

MalagĂ³n et al. [15],

35

AS-GCT

N/A

N/A

Teratoma, yolk sac tumour

N/A

N/A

Orchidectomy (N/A)

N/A

Sahoo et al., [23]

23

AS-GCT, epithelioid

Right flank pain, back pain

Normal

Teratoma

Parenchyma

65 × 60 × 55

Orchidectomy (clear)

No

Steele et al. [22]

24

AS-GCT, epithelioid

Left testis mass (6 months)

Normal

Teratoma, epithelioid angiosarcoma

Parenchyma, rete testis, epididymis, spermatic cord

80 × 70

Orchidectomy (clear)

No

Hughes et al. [20]

16

AS-GCT

Right testis mass (1 months)

Normal

Teratoma, angiosarcoma

Parenchyma

90 × 70 × 65

Orchidectomy (clear) post-op RT

No

Therapy-related angiosarcoma in germ cell tumour

Idrees et al. [7]

38

AS-GCT

Abdominal pain

AFP 8320

Teratoma, yolk sac tumour, seminoma

Parenchyma, epididymis, para-testicular soft tissue

N/A

Orchidectomy (clear)

No

Lee et al. [21]

35

AS-GCT, epithelioid

N/A

N/A

Seminoma

N/A

80

Orchidectomy (clear)

No

Ulbright et al. [6]

17

AS-GCT

Testis mass, back pain (1 years)

N/A

Teratoma

N/A

N/A

Orchidectomy (N/A)

No