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Clinical, dermoscopic and histopathologic findings of retiform hemangioendothelioma.
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PMID:  24282657     Owner:  NLM     Status:  PubMed-not-MEDLINE    
Abstract/OtherAbstract:
Retiform hemangioendothelioma (RH) is an uncommon vascular neoplasm of borderline malignancy that clinically develops as a solitary, gradually enlarging exophytic mass, nodule or plaque, most often on the lower limbs, upper limbs and trunk. Clinical recognition of RH is troublesome because of its non-specific appearance, with differential diagnosis comprising a variety of benign and malignant tumors clinically presenting as reddish nodules. In this article we describe the clinical, dermoscopic and histopathologic findings in a case of RH developing on the flank of a 26-year-old woman, and discuss the possible role of dermoscopy in facilitating the clinical recognition of this rare tumor.
Authors:
Amanda Mota; Giuseppe Argenziano; Iris Zalaudek; Simonetta Piana; Caterina Longo; Elvira Moscarella; Aimilios Lallas
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Publication Detail:
Type:  Journal Article     Date:  2013-10-31
Journal Detail:
Title:  Dermatology practical & conceptual     Volume:  3     ISSN:  2160-9381     ISO Abbreviation:  Dermatol Pract Concept     Publication Date:  2013  
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Created Date:  2013-11-27     Completed Date:  2013-11-27     Revised Date:  2014-01-24    
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Nlm Unique ID:  101585990     Medline TA:  Dermatol Pract Concept     Country:  United States    
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Languages:  eng     Pagination:  11-4     Citation Subset:  -    
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Journal ID (nlm-ta): Dermatol Pract Concept
Journal ID (iso-abbrev): Dermatol Pract Concept
Journal ID (publisher-id): DP
ISSN: 2160-9381
Publisher: Derm101.com
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Copyright © 2013 Mota et al.
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Received Day: 20 Month: 6 Year: 2013
Accepted Day: 09 Month: 7 Year: 2013
collection publication date: Month: 10 Year: 2013
Electronic publication date: Day: 31 Month: 10 Year: 2013
Volume: 3 Issue: 4
First Page: 11 Last Page: 14
PubMed Id: 24282657
ID: 3839825
DOI: 10.5826/dpc.0304a03
Publisher Id: dpc0304a03

Clinical, dermoscopic and histopathologic findings of retiform hemangioendothelioma
Amanda Mota1
Giuseppe Argenziano1
Iris Zalaudek12
Simonetta Piana1
Caterina Longo1
Elvira Moscarella1
Aimilios Lallas1
1Skin Cancer Unit, Arcispedale Santa Maria Nuova IRCCS, Reggio Emilia, Italy
2Department of Dermatology, Medical University of Graz, Austria
All authors have contributed significantly to this publication.
Correspondence: Corresponding author: Aimilios Lallas, M.D., Skin Cancer Unit, Arcispedale Santa Maria Nuova, Viale Risorgimento 80, 42123 Reggio Emilia, Italy. Tel. 00390522295611; Fax. 00390697625822. Email: emlallas@gmail.com

Introduction

Hemangioendothelioma is a term encompassing neoplasms with an intermediate biological behavior between benign hemangiomas and angiosarcomas. It affects the skin and the soft tissues and includes retiform hemangioendothelioma (RH), papillary intralymphatic angioendothelioma (PILA, Dabska’s tumor), epithelioid, kaposiform, pseudomyogenic, and composite hemangioendotheliomas [1].

RH is an infrequently encountered vascular neoplasm of borderline malignancy that was originally classified as a distinct type of low-grade cutaneous angiosarcoma (CA) in 1994 by Calonje et al [2]. Histopathologically, the vascular channels of RH resemble the rete testis (retiform), while the term “hemangioendothelioma” reflects its putative borderline malignancy, as opposed to the benign angioma and the malignant angiosarcoma.

Morphologically, RH typically develops as a solitary, gradually enlarging exophytic mass, nodule or plaque, most often on the lower limbs, upper limbs and trunk. The tumor shows a predilection for young to middle-aged adults (mean age 36 years) and females (2:1) [2]. Duration of the disease and tumor size at the time of diagnosis have been reported to range from 2 months to several years and from 1 to 30 cm, respectively [2]. A case of RH presenting with multiple lesions on the limbs and trunk has also been described [3].

Surgical excision is the treatment of choice for RH [14]. However, accurately defining the excision margins in a vascular neoplasm with a dissecting growth pattern is particularly troublesome. Indeed, the tumor is associated with a high rate of local recurrence (50%), which may occur from months to several years after surgery [2,3]. Regional lymph node metastasis was reported in a single patient, while no distant metastases have been reported to date [4].


Case report

A 26-year-old woman presented with a 2-month history of an asymptomatic, enlarging tumor of the right flank. The patient’s previous medical history was unremarkable. Clinical examination revealed a well-defined, infiltrated red nodule, measuring a diameter of 3 cm (Figure 1). No regional lymphadenopathy was detected. Dermoscopic examination revealed a pinkish background color and few dotted and linear vessels (Figure 2).

Histopathologic examination (Figures 3 and 4) following punch biopsy revealed that the tumor was dermal based and ill defined. It was characterized by an infiltrative growth pattern, involving the entire dermis but sparing the subcutis, and consisted of long and thin arborizing vessels dissecting the dermal collagen. The vessels were lined by plump endothelial cells with frequent hobnail features and papillary projections. Rare solid endothelial areas were present in the superficial part of the lesion. No cytological atypia nor mitotic activity were noted. Extravasation of erythrocytes, hemosiderin deposition and inflammatory infiltrate were absent. On immunohistochemistry, the lesion reacted diffusely with CD31 and focally with D2–40. The monoclonal antibody against the latent nuclear antigen-1 of HHV8 was negative.

Based on the aforementioned histopathologic findings, the diagnosis of RH was established and the tumor was subsequently excised. On histopathology, some residual dissecting vessels were present besides the dermal scar.


Discussion

Clinical recognition of RH is troublesome because of its non-specific appearance, with differential diagnosis comprising a variety of benign and malignant tumors clinically presenting as reddish nodules. RH has to be differentiated from other hemangioendotheliomas, CA, hemangioma, targetoid hemosiderotic hemangioma, blue-rubber bleb nevus syndrome, Kaposi’s sarcoma (KS), lymphoma, dermatofibrosarcoma protuberans, amelanotic melanoma (AM) and cutaneous metastases [2,3].

Although the diagnosis of RH is based on histopathologic examination, discrimination from other vascular tumors might be challenging even histopathologically. The presence of infiltrative vascular spaces allows ruling out benign proliferations as hobnail hemangioma, which typically is more superficial and well defined. Differentiation from Kaposi’s sarcoma (KS) is based mainly on the different clinical setting, the typical cellular spindling and the HHV8 immunoreactivity of the neoplastic cells that characterize KS. CA is characterized by cellular pleomorphism and prominent mitotic activity, features that allow discrimination from RH. Distinguishing between RH and PILA is highly challenging, since they both affect young patients, are characterized by a predilection for the limbs, and share similar histopathologic characteristics [57]. The architecture of the vessels, which are thin and arborizing in RH and often dilated in PILA, and the immunohistochemical reactivity of the latter to markers of lymphatic differentiation like D2–40 and VEGFR-3 represent clues for differentiating between the two entities [7].

In our case, D2-40 antibody reacted only in normal vascular endothelium, representing the internal control, and failed to demonstrate a convincing lymphatic differentiation, findings suggestive of the diagnosis of RH [8,9].

Given that the choice treatment of RH is surgical excision to tumor-free margins, the most relevant differential diagnostic problem in clinical terms, is to discriminate RH from benign vascular tumors, whose management is essentially conservative.

Dermoscopy has been shown to improve the clinical evaluation of pigmented and non-pigmented skin tumors, enabling the visualization of morphologic structures that might be critical for the differential diagnosis [10].

In our case, dermoscopy revealed a pinkish color, which is also known to characterize AM, KS and CA and, effectively, cannot be considered as predictive of a specific diagnosis [10,11]. However, since it has been only described in the context of malignant tumors, the detection of pinkish (milky red) color enhanced us to avoid misinterpretation of the tumor as benign and prompted us to perform a biopsy.

In conclusion, although the dermoscopic criteria of RH and other endotheliomas require further investigation, our case highlights that dermoscopy should always be performed when clinically evaluating skin tumors, since the additional morphologic information provided might facilitate the appropriate clinical decision. Undoubtedly, dermoscopic findings should always be integrated with clinical information, such as patient’s age and history. Furthermore, the current case further supports the previously reported observation that detection of pinkish color on dermoscopy of nodular lesions is suggestive of malignancy and should warrant excision. Finally, RH should be added in the differential diagnostic spectrum when evaluating a red nodule exhibiting a pinkish color under dermoscopy.


Notes

Funding: This study was supported, in part, by the Italian Ministry of Health (RF-2010-2316524.

Competing interests: The authors have no conflicts of interest to disclose.

References
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3.. Duke D,Dvorak A,Harris TJ,Cohen LM. Multiple retiform hemangioendotheliomas. A low-grade angiosarcomaAm J DermatopatholYear: 1996186606108989934
4.. Bhutoria B,Konar A,Chakrabartis S,Das S. Retiform hemangioendothelioma with lymph node metastasis: a rare entityIndian J Dermatol Venereol LeprolYear: 200975160219172034
5.. Fukunaga M,Endo Y,Masui F,et al. Retiform haemangioendotheliomaVirchows ArchYear: 19964284–530148764941
6.. Dabska M. Malignant endovascular papillary angioendothelioma of the skin in childhood: clinicopathologic study of 6 casesCancerYear: 196924503105343389
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8.. Emberger M,Laimer M,Steiner H,Zelger B. Retiform hemangioendothelioma: presentation of a case expressing D2-40J Cutan PatholYear: 20093699879019674202
9.. Parsons A,Sheehan DJ,Sangueza OP. Retiform hemangioendotheliomas usually do not express D2–40 and VEGFR-3Am J DermatopatholYear: 20083031318212541
10.. Zalaudek I,Kreusch J,Giacomel J,et al. How to diagnose non-pigmented skin tumors: a review of vascular structures seen with dermoscopy: part 1. Melanocytic skin tumorsJ Am Acad DermatolYear: 201063336178420708469
11.. Zalaudek I,Gomez-Moyano E,Landi C,et al. Clinical, dermoscopic and histopathological features of spontaneous scalp or face and radiotherapy-induced angiosarcomaAustralas J DermatolYear: 2013543201722943153

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Keywords: retiform hemangioendothelioma, hemangioendothelioma, dermoscopy, vascular tumors.

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