ARTICLE
Auteur(s) : Angel FERNANDEZ-FLORES1, Manuel G.
MONTERO2
1 Histopathology Dept, Clinica Ponferrada, Leon,
Spain
2 Dermatology Dept, Clinica Ponferrada, Leon,
Spain
<gpyauflowerlion@terra.es>
We have read with great interest the report about silica
granulomas [1], and agree with the authors, who wonder why these
lesions are not more common in daily practice, in view of the
ubiquity of silica.
We also recently saw a case in which no history of exposure to
silica could be recorded, and which was interesting because of its
association with a long history of sarcoidosis, since both entities
have been previously related in literature [2-7].
Our patient, a 52-year-old woman, had been diagnosed with a
systemic stage I-sarcoidosis twelve years previously, and was
currently stable with normal clinical parameters.
She went to the Dermatologist, presenting non-tender red and
pearly patches, plaques and nodules, which had appeared on her
knees and elbows, two years before. The biggest lesion was
7 mm in diameter (figure 1A). Some of the
lesions spontaneously regressed. There was no history of
traumatism, injury or professional exposure to silica.
The biopsy of one of the lesions, from an elbow, showed a typical
sarcoidal granulomatous dermatitis (figure 1B), with refractive
particles in the center of the granulomas (figure 1C). No asteroid or
Schaumann bodies were found.
The histochemical study with Giemsa, Ziehl-Neelsen and PAS failed
to show any micro-organisms.
The reason why silica granulomas are not seen more often in daily
practice could be due to their underdiagnosed condition [8], or to
spontaneous resolution. But another possibility is that a
susceptibility to form granulomas, in the patient, is necessary for
these to appear.
In the literature, there is not always a clear relationship
between sarcoidosis and silica granuloma, a subject complicated by
the use of the term scar-sarcoidosis to refer to granulomas
appearing in old scars [4].
Silica particles were a mere contaminant for some [5], but were
considered as a diagnostic clue by many, excluding a sarcoidosis
when present [4, 5, 8].
Several studies have shown how foreign bodies are not an uncommon
finding in cutaneous granuloma of patients with systemic
sarcoidosis [7,8]. This might be due to a tendency to easily
develop granulomas in these patients, either against foreign bodies
[7], or scars.
In conclusion, the term scar-sarcoidosis should only be used, if
ever, when a systemic sarcoidosis is present; and siliceous
particles in a granuloma cannot exclude cutaneous sarcoidosis.
n
1. Bozpete G, Rakhshanfar M, Erkin G, Ozkaya O,
Sahin S. Cutaneous silica granuloma: a lesion that might be
clinically underdiagnosed. Eur J Dermatol 2005; 15:
194-5.
2. Payne CMER, Thomas RHM, Black MM. From silica
granuloma to scar sarcoidosis. Clin Exp Dermatol 1983; 8:
171-5.
3. Camba MIC, Abelaira MDC, Piñeiro MJM, Larrañaga
JRF. La sarcoidosis cutánea cicatricial: el papel del sílice. An
Med Interna 1996; 13: 155.
4. Kim YC, Triffet MK, Gbson LE. Foreign bodies in
sarcoidosis. Am J Dermatopathol 2000; 20: 408-12.
5. Walsh NM, Hanly JG, Tremaine R, Murray S.
Cutaneous sarcoidosis and foreign bodies. Am J Dermatopathol
1993; 15: 203-7.
6. Marcoval J, Mana J, Moreno A, Gallego I, Fortuno
Y, Peyri J. Foreign bodies in granulomatous cutaneous lesions of
patients with systemic sarcoidosis. Arch Dermatol 2001; 137:
427-30.
7. Val-Bernal JF, Sanchez-Quevedo MC, Corral J,
Campos A. Cutaneous sarcoidosis and foreign bodies: an electron
probe roentgenographic microanalytic study. Arch Pathol Lab
Med 1995; 119: 471-4.
8. Mowry RG, Sams WM Jr, Caulfield JB. Cutaneous
silica granuloma; a rare entity or rarely diagnosed?: report of two
cases with review of the literature. Arch Dermatol 1991;
127: 692-4.
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