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Palpebral hidrocystomas are benign tumors also known as cystic apocrine adenoma, cyst of sweat gland, apocrine retention cyst or cyst of Moll. They originate from eccrine or apocrine sweat glands and often occur on the face and the eyelids. Other atypical locations such as the chest, the shoulders and the foreskin have been reported. Hidrocystoma is a small translucent, shiny cyst. It appears as single or multiple cystic lesion. Their histogenesis is uncertain. Indeed, apocrine hidrocystoma could arise from the residuals of the primitive apocrine glands or of the gland of Moll. The eccrine hidrocystoma could arise from the eccrine glands or the excretory duct of the glands of Moll. Their clinical differentiation is little obvious and diagnosis is based on histological examination. They are characterized by two clinical presentations: isolated hidrocystomas and the associated types. Isolated hidrocystoma is the most common type: hidrocystoma appears as single or multiple cystic lesions and it is not associated with extraocular signs. Apocrine hidrocystomas are solitary in 93% of cases while eccrine hidrocystomas appear most often as multiple lesions. The associated types are more rare and have been only described for the multiple hidrocystomas. If in the majority of cases a treatment based on argon laser is sufficient, more voluminous hidrocystomas require surgical resection. We here report the case of a young patient presenting with translucent nodule in the external canthus of the left eye. Hidrocystoma, molluscum pendulum and syringoma were the suspected diagnoses. Surgical resection was performed as well as histologic examination which confirmed the diagnosis of hidrocystoma.

Tubulo-papillary apocrine adenoma (TAA) is a very rare sweat gland tumor. TAA in association with syringocystadenoma papilliferum (SCP) is exceptional. A 2-year-old Tunisian child developed a mixed tumor on the scalp: TAA in association with SCP. Histologically, the tumor consisted of dilated duct-like areas with some apocrine gland-like areas. The superficial part of the tumor was connected to the epidermis and showed the characteristics of SCP. The characteristics and differences in histopathologic and immunohistochemical findings in this mixed tumor are described., (Copyright © 2016 Elsevier Masson SAS. All rights reserved.)

Background: Eccrine porocarcinoma is a rare cutaneous tumor arising from the intra-epidermal portion of eccrine sweat glands, the acrosyringium. Histoprognostic studies in large series are rare. Herein, we report a retrospective study of 50 cases., Patients and Methods: Fifty cases of porocarcinoma were retrieved from a histopathological register. Each histopathological sample was evaluated for the following criteria: presence or absence of dermal invasion, pattern of the infiltrative component (pushing or infiltrative), tumor thickness, lymphovascular emboli, perineural invasion and mitotic index. Clinical data and outcome were also retrieved for each patient., Results: Mean patient age was 77 years (range: 43-99 years). The mean duration of progression prior to diagnosis was 4 years and 5 months. The 2 most common skin locations were the head (38%) and lower limbs (20%). The lesions showed no specific distinctive clinical features. Six cases were in situ, and 44 were invasive (23 with limited infiltration and 20 with scattered infiltration). Mean tumor thickness was 4.37 mm (range: 0.5 to 20 mm). Neighboring or remote epidermal involvement was noted in 7 cases. Lymphovascular emboli were observed in 3 cases. No cases of neurotropism were observed. The average mitotic index was 6.5 mitoses/high power (×400) field. A mean follow-up of 24.3 months was available for 48 patients. Local recurrence was noted in 5 patients, 4 of whom died from visceral metastases. These 5 cases showed no distinctive clinical features, a scattered pattern of the invasive component, cuticular cells, significant tumor thickness (mean 12.8 mm, range 9-20 mm), and an elevated mitotic index. Two histopathological criteria were significantly associated with a metastatic outcome: scattered pattern of the dermal invasive component (P=0.04) and significant tumor thickness, above 10mm (P<0.01)., Conclusion: Porocarcinoma is a tumor without any particular clinical criteria to distinguish it from squamous cell carcinoma. The architecture of the invasive component and tumor thickness constitute 2 important histoprognostic criteria., (Copyright © 2013 Elsevier Masson SAS. All rights reserved.)

Background: Apocrine carcinoma of the skin (ACS) is a rare adnexal neoplasm presenting as an indurated slow-growing dermal or subcutaneous plaque that often occurs in the axilla. Histological distinction between ACS and cutaneous metastases of breast carcinoma may be difficult., Observation: A 64-year-old man presented with a slowly growing left axillary mass, which he had noticed for 2 years, without any other functional or clinical symptoms. Histological examination of the skin biopsy showed dermal invasion with atypical cells in an "Indian file" pattern. The pattern of the tumour and immunohistochemical staining suggested a diagnosis of breast carcinoma metastasis. However, the history of a slow-growing tumour and negative initial testing for a primary adenocarcinoma supported the hypothesis of ACS., Discussion: A 100 cases of ACS have been reported in the literature with the main site being the axillary area. The differential diagnostic between axillary ACS and metastasis of lobular breast carcinoma has been discussed recently. Diagnosis may be difficult since the pattern of the tumour can be misleading and immunomarkers are not always specific., Conclusion: We report a new case of axillary ACS histologically mimicking lobular breast carcinoma metastasis., (Copyright 2010 Elsevier Masson SAS. All rights reserved.)

The eccrine poroma is a rare benign sudoral tumour, which creates a fleshy formation. The diagnosis is made according to the anatomopathological study. The usual site is the sol, but in rare cases, other sites have also been reported. The authors report three cases of eccrine poroma localised in the scalp with literature review.

The vast majority of palpebral tumors are benign and, when complete, straightforward excision is curative. In some cases, laser ablation can be appropriate. These tumors originate from the pilosebaceous adnexa of the skin and are mainly composed of cysts. For carcinomas, the extent of the tumoral expansion must be assessed on pathological examination of a specimen. In case of recurrence, the tumor may extend beyond the clinically visible borders. This is particularly true in the sclerodermiform type of basal cell carcinoma, which invades tissues deeply, in spindle cell carcinoma, which spreads within the thickness of the epidermis or the conjunctival epithelium, and in sebaceous gland carcinoma, which can present in a masquerade fashion.

A cystic cutaneous mass was observed on the lateral canthus of the left eyelid in a 25-year-old woman, 2 years after being operated on for a lesion that had existed in the same area several years before, but the patient could not identify its nature. The present mass appeared as a well-circumscribed bluish cystic lesion. A surgical resection was performed; pathological analysis disclosed a cystic sweat tumor composed of several contiguous cysts. One year of follow-up has revealed no complications.

Background: Porocarcinoma is a malignant tumour of the eccrine sweat duct, arising from acrosyringium. The tumoral lesions involve the deep dermal tissue., Case Report: We report the case of an 84 year-old woman, suffering from a porocarcinoma, extensively involving the major part of the left lower limb. The first symptoms appeared two years ago. Hundreds of metastatic papules and small nodules were present, isolated or confluent into large plaques. The clinical picture was very close to lymphangioma. Diagnosis was confirmed by histopathologic examination. Radiotherapy was useful short-term, allowing partial flattening of the lesions and improving lymphatic drainage, thus providing comfort for the patient. It did not prevent a later progression of the tumoral process., Discussion: Porocarcinoma is a rare tumour that usually appears as a single nodule or a plaque, arising from a preexistent eccrine poroma, or developing de novo. Two histopathological variants are described: trabecular or epidermotropic. This latter form, observed in the present case, is more aggressive, leading to frequent local recurrences and/or metastases. Our report is exceptional: the literature shows only one other case with such widespread cutaneous involvement. The clinical course of our case is discussed.

A clinico-pathologic case of a black hidrocystoma of the left eyelid margin is reported in a 45-year-old female patient. Clinically, a black nodule was disclosed after eversion of the superior left lid. A surgical full thickness eyelid focal resection was performed to remove the cyst. Histopathology found a cyst covered with an epithelium with a double layer of cells and filled with a brownish granular content, typical of a black hidrocystoma.

Introduction: We report a new case of eccrine carcinoma with mucinous stroma characterized by its voluminous exophytic growth., Case Report: An 80-year-old patient was hospitalized for a voluminous vegetating tumor localized over the left temporal region and which had developed over the 10 preceding years. Wide exeresis was performed and histology confirmed the diagnosis of eccrine carcinoma. No locoregional recurrence was noted 18 months later., Discussion: Eccrine carcinoma with mucinous stroma, also termed eccrine mucinous adenocarcinoma, is a rare adnexal skin carcinoma usually localized on the face or scalp. Abundant zones of mucine are characteristic dissociating a dermal cell proliferation with ruban architecture. The volume of the tumor in our case was particularly remarkable although outcome was favorable after surgical treatment.

Syringocystadenoma papilliferum is an infrequent hamartoma of the sweat glands, usually of the scalp or temporal area. We observed a syringocystadenoma papilliferum in a young patient from Senegal. The lesion was unique and presented as a round 4 cm plaque with a red smooth surface. The diagnosis was based on the histologic examination. Complete surgical exeresis was performed. Localization on the knee is very unusual.

The ceruminous glands tumors are very rare pathologies, being even rarer their origin other then the external auditory canal. In this paper, we report a case of ceruminous adenoma of the middle ear and study other 125 cases related in the literature since 1941. We analyze the incidence of each hystological type, the sex, race, age and site of origin of the tumors.

Tubular apocrine adenoma is a rare, benign apocrine tumour of the skin, histologically distinct from other epithelial proliferations, showing apocrine differentiation. A new case of this uncommon lesion is reported herein and a review of the literature concerning this tumour is made.

It appears justified to isolate under the term syndrome of Nicolau and Balus', a group of deformities that include eruptive syringomas of the disseminated micropapular type, milium cysts and atrophoderma vermiculata. We present here a highly typical observation of an 11-year-old child whose mother also presented with eruptive syringomas. This syndrome accentuates the semiological value of disseminated syringomas and atrophoderma vermiculata, which often occur in the context of a complex syndrome. In addition, an associated elastopathy was discovered by light- and electron-microscopic observations.