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Primary epithelioid angiosarcoma of the chest wall complicating calcified fibrothorax and mimicking empyema necessitates

We describe the case of a 72-year-old male patient with primary epithelioid angiosarcoma of the chest wall (PEACW). The patient complained of a painful lump in his chest. His medical history was consistent with calcified fibrothorax secondary to a tuberculous infection during childhood. Empyema necessitatis (EN) was initially suspected. An X-ray of the chest (Figure 1A) showed characteristics similar to those seen on previous X-rays. A CT scan demonstrated a heterogeneous mass that focally destroyed a rib and invaded chest wall muscles (Figure 1B). A CT-guided biopsy of the mass (Figure 1C) revealed a high-grade PEACW. Unfortunately, the patient died from brain and pulmonary metastases three weeks later.

Figure 1
In A, a posteroanterior chest X-ray showing right calcified fibrothorax (asterisks). In B, axial contrast-enhanced CT of the chest scan showing a heterogeneous hypervascular mass (asterisk) infiltrating the right serratus anterior and pectoralis muscles, as well as the fourth rib (long arrow). Note the extensive calcified fibrothorax on the right. In C, axial CT of the chest, with maximum intensity projection, showing a large-core needle biopsy (14-gauge) traversing the chest wall for histological analysis of the mass (asterisk)

The development of a chest wall lump in a patient with chronic calcified fibrothorax of tuberculous origin should prompt the possibility of EN. However, only a few cases of PEACW developing in patients with a chronic calcified fibrothorax have been published in the literature.11. Hattori H. Epithelioid angiosarcoma arising in the tuberculous pyothorax: report of an autopsy case. Arch Pathol Lab Med. 2001;125(11):1477-9.

2. Maziak DE, Shamji FM, Peterson R, Perkins DG. Angiosarcoma of the chest wall. Ann Thorac Surg. 1999;67(3):839-41. https://doi.org/10.1016/S0003-4975(99)00073-9
https://doi.org/10.1016/S0003-4975(99)00...
-33. Aozasa K, Naka N, Tomita Y, Ohsawa M, Kanno H, Uchida A, et al. Angiosarcoma developing from chronic pyothorax. Mod Pathol. 1994;7(9):906-11. To our knowledge, there have been no reported cases in which PEACW complicating calcified fibrothorax was accurately diagnosed on the basis of percutaneous biopsy. Despite its rarity, PEACW should be suspected in patients with chronic calcified fibrothorax that develops as a chest wall mass.

RECOMMENDED READING

  • 1
    Hattori H. Epithelioid angiosarcoma arising in the tuberculous pyothorax: report of an autopsy case. Arch Pathol Lab Med. 2001;125(11):1477-9.
  • 2
    Maziak DE, Shamji FM, Peterson R, Perkins DG. Angiosarcoma of the chest wall. Ann Thorac Surg. 1999;67(3):839-41. https://doi.org/10.1016/S0003-4975(99)00073-9
    » https://doi.org/10.1016/S0003-4975(99)00073-9
  • 3
    Aozasa K, Naka N, Tomita Y, Ohsawa M, Kanno H, Uchida A, et al. Angiosarcoma developing from chronic pyothorax. Mod Pathol. 1994;7(9):906-11.

Publication Dates

  • Publication in this collection
    Jan-Feb 2017
Sociedade Brasileira de Pneumologia e Tisiologia SCS Quadra 1, Bl. K salas 203/204, 70398-900 - Brasília - DF - Brasil, Fone/Fax: 0800 61 6218 ramal 211, (55 61)3245-1030/6218 ramal 211 - São Paulo - SP - Brazil
E-mail: jbp@sbpt.org.br