Acta Dermato-Venereologica 99-4CompleteContent | Page 23
450
SHORT COMMUNICATION
Disfiguring Nodular Cephalic Xanthoma Disseminatum: An Exceptional Variant of a Forgotten Entity
Arturo BONOMETTI 1 , Jessica GLIOZZO 2 *, Chiara MOLTRASIO 2 , Filippo BAGNOLI 3 , Luigia VENEGONI 4 , Emanuela PASSONI 2 ,
Marco PAULLI 1 and Emilio BERTI 2,4
Unit of Anatomic Pathology, Department of Molecular Medicine, IRCCS San Matteo Foundation, University of Pavia, Pavia, 2 Unit of Dermatology,
Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Via Pace 9, Milan, 3 Department of Oncology and Hematology, and 4 Department
of Pathophysiology and Organ Transplantation, University of Milan, Milan, Italy. E-mail: [email protected]
1
Accepted Jan 7, 2019; E-published Jan 9, 2019
Xanthoma disseminatum (XD) is an extremely rare cu-
taneous, normolipidemic, proliferative disorder of the
Mononuclear Phagocyte System. It was first described
by Von Gräfe and Virchow but recognized as a distinct
entity by Montgomery & Osterberg in 1938 (1). Approx-
imately 140 cases are reported in the English literature.
Clinically, XD is characterized by a symmetrical skin
eruption of reddish papules or nodules, with predilec-
tion for the head, neck, flexural and intertriginous areas.
These lesions, initially isolated, tend to slowly merge
into large yellowish plaques, during years. The mean
age at presentation is 30 years and male cases outnumber
female ones by a ratio of 2:1. XD is generally thought to
be a benign disorder with a chronic progressive course
(2–4). Caputo et al. (5) recognized 3 clinical variants of
XD: 1) a self-healing form; 2) a persistent form and 3)
a progressive multi-system (MS) form. The report rate
of this entity is becoming even lower now than in past
years, perhaps due to its high diagnostic overlap with
Erdheim-Chester Disease (ECD) (6, 7).
CASE REPORT
We hereby describe the case of a previously healthy 47-year-old
Caucasian woman presented to our attention in January 2011,
with a 2-year long history of cephalic xanthomas. Her lesions
consisted of yellow periocular and perioral plaques extending to
the zygomatic area as well as small yellow hard-elastic nodules
growing next to the inner canthi (Fig. 1). Complete radiological,
hematological (blood count, metabolic, renal and liver functions/
profiles) and endocrinological examinations all tested negative and
failed to reveal any systemic involvement. During the following
7 years, the lesions displayed a slow but progressive extension
with symmetrical involvement of the whole face (Fig. 1). She
never developed diabetes insipidus or any other signs of systemic
involvement. Previous therapies (hydroxychloroquine and cyclo
phosphamide) and surgeries (including CO 2 laser therapy) led to
constant recurrences and subsequent regrowth of lesions, together
with surgery-related keloid scars, resulting in high mechanical,
psychological and sociological impairment. Skin biopsy (Fig. 1)
showed a polymorphic dense upper- and mid-dermal infiltration
consisting of large histiocytes, admixed with few lymphocytes and
neutrophils. Histiocytes were mostly characterized by large nuclei
often with prominent nucleoli and an abundant pale cytoplasm.
Foamy, Touton and Langhans cells were also present, focally in
large numbers. There were no signs of epidermotropism. Immu-
nohistochemical profile of the histiocytes was positive for CD4,
CD11c, CD14, CD68/PGM1, CD163, fXIIIa, vimentin, lysozyme,
fascin but tested negative for CD1a, CD34 and CD207/langerin.
Ki-67 stained 1–5 % of the cells. BRAF V600E analysis failed to
reveal any alteration. Sixteen years after the first manifestation,
the patient is alive and in a good clinical condition, although with
chronic persistent evolution of the disfiguring lesions.
Informed consent was obtained in accordance with local ethical
guidelines and with the Helsinki Declaration of 1975.
DISCUSSION
Histiocytoses have recently been reclassified in 5 dif-
ferent groups based on a combination of clinical, ra-
diographic, histopathological and molecular findings.
XD belongs to the “xanthogranuloma-family” of the
C(utaneous)-group, due to its prevalent skin involvement
Fig. 1. Clinical and histopatho
logical features of the patient. The
patient came to our attention with
yellowish plaques limited to periocular
and perioral regions (A, C). During
the first 2 years of follow-up the
lesions slowly increased in volume and
extended to columella (D) and after 5
years they presented as thick tumor/
nodular lesions and confluent plaques
extending to the forehead, zygoma,
eyelids, outer nostrils and mentolabial
sulci (B, E). Skin biopsy revealed a
dense and polymorphic histiocytic
infiltrate (F) made up of large cells with
abundant and often foamy cytoplasm
(G) and multinucleated giant cells of
the Touton (H) and Langhans type,
admixed with small lymphocytes and
neutrophils.
doi: 10.2340/00015555-3111
Acta Derm Venereol 2019; 99: 450–451
This is an open access article under the CC BY-NC license. www.medicaljournals.se/acta
Journal Compilation © 2019 Acta Dermato-Venereologica.