Diffuse Dermal Angiomatosis Arising in Cutis Marmorata Telangiectatica Congenita

Halbesleben, Jennifer J.; Cleveland, Mark; Stone, Mary Seabury

doi:10.1001/archdermatol.2010.331

Cited by 5 publications

(5 citation statements)

References 7 publications

(7 reference statements)

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“…Other reported diseases associated with this cutaneous reactive pattern include Takayasu arteritis, calciphylaxis, hepatitis, monoclonal gammopathy, and cutis marmorata telangiectatica congenita. 2, [7][8][9] There is also a reported association with COPD, which was present in our patient as well. Pulmonary function impairment due to COPD, obstructive sleep apnea, and obesity hypoventilation syndrome may contribute to the tissue hypoxia seen in DDA.…”

Section: Discussionsupporting

confidence: 81%

Diffuse dermal angiomatosis localized to abdominal striae

Frizzell

Shah

Parekh

2020

Baylor University Medical Center Proceedings

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Diffuse dermal angiomatosis is a rare, benign, reactive cutaneous vascular disorder considered to be a distinct variant of reactive angioendotheliomatosis. The disease typically presents in obese patients who smoke and have atherosclerotic risk factors, vasculopathies, or other comorbidities associated with hypoxemia. We present a case of a 40-year-old woman with ulcerated plaques on her abdomen consistent with diffuse dermal angiomatosis on histopathological evaluation. Unique to our patient was localization of the lesions to the abdominal striae.

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Section: Discussionsupporting

confidence: 81%

Diffuse dermal angiomatosis localized to abdominal striae

Frizzell

Shah

Parekh

2020

Baylor University Medical Center Proceedings

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“…Additional vascular anomalies, especially capillary malformations such as port-wine stain, were reported frequently. 25,[40][41][42][43][44] According to this, in Kienast's study were found 15% of vascular anomalies, 50% of which were capillary malformations. 3 Neurological abnormalities have been described, such as neonatal hypotonia, developmental delay, mental retardation and seizures.…”

Section: Discussionmentioning

confidence: 86%

“…18 In 2006 Torrelo reported two children with CMTC and extensive Mongolian spots but he hypothesized it represented a distinct form of phacomatosis pigmentovascularis. 41 Our patient had face erythema, most pronounced in the upper 2/3, a large teleangiectasic-erythematous patch that affected the front right hemithorax (Fig.1), erythema and telangiectasias scattered on cervicothoracic and lumbosacral spine (Fig.2), an extensive teleangiectasic-erythematous patch on the lateral surface of the right leg, at the level of knee, with a few small areas of atrophy (Fig.3); upper limbs and contralateral lower limb showed livedo reticularis more evident during environmental temperature exposure. Foot sole, especially on lateral side, appeared erythematous (Fig.4).…”

Section: Discussionmentioning

confidence: 99%

Cutis Marmorata Telangiectatica Congenita in a Preterm Female Newborn: Case Report and Review of the Literature

et al. 2014

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RiassuntoLa Cutis Marmorata Telangiectatica Congenita (CMTC) è una condizione rara, di solito presente alla nascita, caratterizzata da cutis marmorata persistente, localizzata o generalizzata, telangectasia e flebectasia. Riportiamo il caso di una neonata pretermine, terzogenita di genitori caucasici non consanguinei, con CMTC alla nascita che mostrava le tipiche lesioni cutanee e glaucoma congenito monolaterale. La patogenesi di questo disordine non è nota e la causa è probabilmente multifattoriale. Come fattori etiologici sono stati ipotizzati l'esposizione ad agenti teratogeni ed un meccanismo di trasmissione autosomico dominante a penetranza incompleta. La prognosi, nei casi senza complicazioni, è buona. AbstractCutis Marmorata Telangiectatica Congenita (CMTC) is a rare, sporadic condition usually present at birth characterized by localized or generalized persistent cutis marmorata, telangiectasia and phlebectasia. We report a preterm female newborn, the third child of non-related caucasian parents, with CMTC at birth who showed typical cutaneous features and monolateral congenital glaucoma. The pathogenesis of this disorder is unknown and the cause is probably multifactorial.Teratogens and autosomal dominant mode of inheritance with incomplete penetrance have been considered as etiological factors. Prognosis, in uncomplicated cases, is good. Case reportM.R. is a female newborn spontaneously delivered at 33 weeks and 5 days of gestational age (GA) for maternal preeclampsia. The baby needed no resuscitation at birth. Apgar score was 9-9 at 1' and 5' minutes of life respectively. Family medical history was noncontributory. During first hours of life, for incoming of respiratory distress syndrome, exogenous porcine surfactant was administered and mechanical ventilation performed for about 24 hours. Hypoglycemia was corrected by infusion of 10% glucose solution through umbilical venous catheter. Since birth marbled bluish and deep purple reticulated skin lesions involving the whole body were noted. The lesions were prominent over the trunk and face but more pronounced over the limbs and became more visible with crying and exposure to room temperature (Fig.1). Clinical characteristics and persistence of cutis marmorata prompted the diagnosis of Cutis Marmorata Telangiectatica Congenita (CMTC). The baby had normal face, head circumference 32.5 cm (90° percentile), birth weight 2,688 Kg (>97° percentile), length 48 cm (>97° percentile), without other vascular anomalies or asymmetry of limbs growth. Neurological examination showed mild hypotonia of the trunk, poor spontaneous motor activity, autonomic instability and immaturity of the organization of behavioral states, while ophthalmological evaluation detected unilateral congenital glaucoma in the left eye. Cardiac examination, audiologic screening, Magnetic Resonance Imaging (MRI) and abdominal ultrasound were normal. At four month of life, under general anesthesia, she underwent surgical trabeculotomy ab externo in the left eye with uneventful postoperative cours...

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“…After excluding cases with explicit unifocal involvement, involvement of both breasts, or un-reported location, 13 cases were found in the literature of DDA with multifocal involvement (1,(4)(5)(6)(7)(8)(9)(10)(11)(12)(13)(14), as in our case (Table SI 1 ). Among them, 84.6% involved women, with mean age 58 years; 46.2% involved current smokers; and 46.2% featured atherosclerosis, as expected according to the review of Touloei et al (3) The thigh was the most common location, observed in 61.5% of cases.…”

Section: Multifocal Diffuse Dermal Angiomatosis: a Reflection Of High Cardiovascular Riskmentioning

confidence: 85%

Multifocal Diffuse Dermal Angiomatosis: A Reflection of High Cardiovascular Risk

Vanhaecke¹,

Sanchez²,

Durlach³

et al. 2020

Acta Derm Venereol

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Diffuse Dermal Angiomatosis Arising in Cutis Marmorata Telangiectatica Congenita

Cited by 5 publications

References 7 publications

Diffuse dermal angiomatosis localized to abdominal striae

Diffuse dermal angiomatosis localized to abdominal striae

Cutis Marmorata Telangiectatica Congenita in a Preterm Female Newborn: Case Report and Review of the Literature

Multifocal Diffuse Dermal Angiomatosis: A Reflection of High Cardiovascular Risk

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