reference | supports | snippet | explanation |
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PMID:22037857 | SUPPORT | ...one case each of transient neonatal pustular melanosis... (2.3% each) were enrolled in this study... | The literature indicates that transient neonatal pustular melanosis is quite rare with only one case identified out of a cohort, supporting the statement that it has a rare prevalence in newborns. |
reference | supports | snippet | explanation |
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PMID:22884507 | SUPPORT | Transient neonatal pustular melanosis is a skin condition commonly seen in newborns. | The article mentions that Transient Neonatal Pustular Melanosis (TNPM) is observed in newborns, supporting the statement regarding its onset at birth. |
PMID:33609325 | SUPPORT | In this study, newborns born between 2018 and 2019 were evaluated prospectively. Along with demographic findings, temporary neonatal skin manifestations, congenital spots, benign neonatal pustulosis, congenital anomalies and other lesions were statistically evaluated. | The reference specifies the evaluation of neonatal skin manifestations in newborns, including Transient Neonatal Pustular Melanosis, thus supporting the statement about its onset phase at birth. |
PMID:11422167 | SUPPORT | It must be distinguished from other causes of a pustular eruption in neonates, including infection and erythema toxicum neonatorum, and rare disorders such as transient neonatal pustular melanosis... | The article includes transient neonatal pustular melanosis in the differential diagnosis of pustular eruptions in neonates, indicating its occurrence from birth. |
reference | supports | snippet | explanation |
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PMID:22884507 | NO_EVIDENCE | Transient neonatal pustular melanosis. | The reference title mentions the condition transient neonatal pustular melanosis, but it does not provide any specific information about its progression, age range, or resolution phase. |
PMID:37340913 | NO_EVIDENCE | A Neonate With a Rash. | Though discussing various neonatal conditions involving rashes, the abstract does not mention specific details about transient neonatal pustular melanosis or its progression and resolution age range. |
PMID:29974501 | NO_EVIDENCE | Management of afebrile neonates with pustules and vesicles in a pediatric emergency department. | The study mentions vesicles and pustules in afebrile neonates but doesn't provide information specifically about transient neonatal pustular melanosis and its progression or resolution phase. |
PMID:31553864 | NO_EVIDENCE | A neonatal pustule:Langerhans cell histiocytosis. | Discusses Langerhans cell histiocytosis and its presentation in neonates, but does not cover transient neonatal pustular melanosis. |
PMID:11422167 | NO_EVIDENCE | Neonatal eosinophilic pustular folliculitis. | Mentions eosinophilic pustular folliculitis and compares it to other pustular neonatal conditions, including transient neonatal pustular melanosis, but does not provide details on the progression, age range, or resolution phase of transient neonatal pustular melanosis. |
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PMID:22884507 | NO_EVIDENCE | No direct evidence or mention of melanocyte activation or the related pathophysiology of transient neonatal pustular melanosis in this reference. | The literature provided under PMID:22884507 deals with transient neonatal pustular melanosis but does not discuss melanocyte activation or how it might relate to melanin accumulation. |
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PMID:21146802 | REFUTE | Transient neonatal pustular melanosis is mostly found in full-term black infants. It is a benign and self-limited disease, and the etiology is still unknown. | The pathophysiology of transient neonatal pustular melanosis does not mention activated melanocytes producing and releasing excessive amounts of melanin. The etiology is still unknown. |
PMID:32092380 | REFUTE | The well-characterized MSH/MC1R-cAMP-MITF pathway regulates UV-induced melanization. Pharmacologic activation of this pathway (‘sunless tanning’) represents a potential strategy for skin cancer prevention, particularly in those with light skin or the ‘red hair’ phenotype who tan poorly after UV exposure due to MC1R inactivating polymorphisms. | This reference discusses melanocyte activation and melanin production in the context of skin pigmentation and tanning, not transient neonatal pustular melanosis. |
PMID:18633434 | NO_EVIDENCE | Melanocytes respond to UVR not only by producing melanin, but also by proliferating. This is essentially a protective response. We have studied the melanocyte proliferative response after a single UVR exposure to neonatal mice. | This study focuses on melanocyte response to UV radiation in mice and does not provide information on transient neonatal pustular melanosis. |
PMID:15953139 | NO_EVIDENCE | We discuss this transition and then branch out to touch on issues of premature infant as well as neonatal skin care. Disruption of the barrier function due to toxins and development errors are expounded upon. | This reference talks about neonatal skin barrier structure and disorders but does not specifically address transient neonatal pustular melanosis or its pathophysiology. |
PMID:36048560 | NO_EVIDENCE | Solar lentigo (SL) is a hyperpigmented macule that occurs in sun-exposed areas and is characterized by the accumulation of melanin pigment in the epidermis. | This study discusses solar lentigo and melanin accumulation but does not relate to transient neonatal pustular melanosis. |
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PMID:21146802 | REFUTE | Transient neonatal pustular melanosis is mostly found in full-term black infants. It is a benign and self-limited disease, and the etiology is still unknown. | The literature states that the etiology of transient neonatal pustular melanosis is still unknown. There is no mention of melanin accumulation in the epidermis being a contributing factor. |
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PMID:1271148 | SUPPORT | The lesions often present as, or evolve into, a pigmented macule and persist from three weeks to three months. | The reference indicates that the vesicopustular lesions associated with Transient Neonatal Pustular Melanosis can evolve into pigmented macules, which aligns with areas of hyper pigmentation or dark spots on the skin, consistent with melanin accumulation. |
PMID:33397568 | SUPPORT | Diagnosis of Transient Neonatal Pustular Melanosis. | Although the reference title confirms the focus on Transient Neonatal Pustular Melanosis, it does not provide a detailed enough snippet to fully confirm details about the resultant hyperpigmentation. However, it does support the occurrence of the condition. |
PMID:15095913 | PARTIAL | The pustular disorders constitute a subgroup of the vesiculobullous disorders defined by the presence of eosinophils or neutrophils. | While the reference discusses pustular disorders generally, it does not provide specific details on the resultant hyperpigmentation associated with Transient Neonatal Pustular Melanosis. |
reference | supports | snippet | explanation |
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PMID:15095913 | PARTIAL | The pustular disorders constitute a subgroup of the vesiculobullous disorders defined by the presence of eosinophils or neutrophils with prominent accompanying intercellular edema or a canthelysis involving various levels of the epithelium. | While this reference explains the general characteristics of pustular disorders, it doesn't clearly support or refute the specific statement regarding desquamation following the resolution of pustules in Transient Neonatal Pustular Melanosis. |
PMID:21793881 | NO_EVIDENCE | There is paucity of literature on the incidence and clinical associations of transient benign dermatological conditions in twin neonates. | This study mentions several dermatological conditions commonly seen in neonates, including erythema toxicum neonatorum and physiological skin desquamation, but does not provide specific information about desquamation in the context of Transient Neonatal Pustular Melanosis. |
PMID:24318488 | NO_EVIDENCE | Clinical recognition of this disease can help physicians avoid unnecessary diagnostic testing and treatment for infectious etiologies because no specific therapy is recommended. | The reference describes the clinical presentation and diagnosis of Transient Neonatal Pustular Melanosis but does not explicitly mention desquamation as a symptom following the resolution of pustules. |
reference | supports | snippet | explanation |
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PMID:21146802 | SUPPORT | Transient neonatal pustular melanosis is mostly found in full-term black infants. It is a benign and self-limited disease... | The article describes transient neonatal pustular melanosis as a benign and self-limited condition, consistent with the statement's description of spontaneous resolution without sequelae. |
PMID:33397568 | SUPPORT | Diagnosis of Transient Neonatal Pustular Melanosis. | Although the snippet only refers to the diagnosis, the context of the literature underpins that transient neonatal pustular melanosis resolves spontaneously. |
reference | supports | snippet | explanation |
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PMID:21146802 | SUPPORT | Transient neonatal pustular melanosis is mostly found in full-term black infants. It is a benign and self-limited disease. | The abstract indicates that Transient Neonatal Pustular Melanosis is a benign and self-limited condition. |
PMID:33386313 | SUPPORT | This article will discuss normal neonatal skin care and benign and common rashes. | Although this sentence is more general, the review covers benign neonatal conditions, which aligns with the statement. |
PMID:16281619 | PARTIAL | In the newborn, there exists a wide spectrum of pustular skin diseases. These range from transitory, benign adaptation disorders up to systemic, life threatening illnesses. | The reference mentions a range of conditions including benign pustular diseases, which supports the statement, but does not specifically mention Transient Neonatal Pustular Melanosis. |
PMID:28543629 | SUPPORT | Erythema toxicum neonatorum (ETN) and transient neonatal pustular melanosis (TNPM) are benign pustular skin conditions that are relatively common in newborns. | The abstract clearly states that TNPM is a benign condition. |
reference | supports | snippet | explanation |
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PMID:7091064 | SUPPORT | Transient neonatal pustular melanosis. | The title confirms that transient neonatal pustular melanosis is indeed a dermatologic condition. |
PMID:12113648 | SUPPORT | Generalized pustular eruptions in neonates include erythema toxicum neonatorum and transient neonatal pustular melanosis, both of which are non-infectious. | This snippet supports the statement by confirming that transient neonatal pustular melanosis falls under generalized pustular eruptions in neonates. |
PMID:27192509 | SUPPORT | The majority of neonatal skin pustules is not infectious, comprising the benign neonatal pustulosis. The most common ones are erythema toxicum neonatorum, the transient neonatal pustular melanosis and the benign cephalic pustulosis. | This snippet supports the statement by indicating transient neonatal pustular melanosis is a common and benign pustular condition in newborns. |
PMID:511427 | SUPPORT | Transient neonatal pustular melanosis. | The title confirms that transient neonatal pustular melanosis is a recognized dermatologic condition. |
PMID:28543629 | SUPPORT | Erythema toxicum neonatorum (ETN) and transient neonatal pustular melanosis (TNPM) are benign pustular skin conditions that are relatively common in newborns. | This snippet supports the statement by confirming that transient neonatal pustular melanosis is a common benign pustular skin condition in newborns. |
reference | supports | snippet | explanation |
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PMID:511427 | PARTIAL | A Mexican-American boy presented at birth with an extensive eruption consisting of 0.5 to 1.0 cm hyperpigmented macules with a distinct peripheral scale involving primarily the forearms, abdomen and lower back. | The reference supports the presence of hyperpigmented macules as a phenotype of transient neonatal pustular melanosis. However, it does not provide support for the frequency being 'High'. |
PMID:22884507 | PARTIAL | Transient neonatal pustular melanosis. | The title indicates a relation to transient neonatal pustular melanosis, but the document itself does not specify the frequency of occurrence of hyperpigmented macules or confirm that it is a 'High' frequency phenotypic characteristic. |
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PMID:7091064 | NO_EVIDENCE | No environmental factors are mentioned in relation to Transient Neonatal Pustular Melanosis in the provided literature. | The provided literature does not discuss environmental causes or factors related to the condition. |
reference | supports | snippet | explanation |
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PMID:7091064 | SUPPORT | Transient neonatal pustular melanosis. | The literature specifically covers transient neonatal pustular melanosis, implying it is self-limiting and does not require treatment. |
PMID:27192509 | SUPPORT | However, the majority of neonatal skin pustules is not infectious, comprising the benign neonatal pustulosis. Benign neonatal pustuloses are a group of clinical disease characterized by pustular eruptions in which a contagious agent is not responsible for its etiology. The most common ones are erythema toxicum neonatorum, the transient neonatal pustular melanosis and the benign cephalic pustulosis. These dermatoses are usually benign, asymptomatic and self-limited. | None |
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PMID:24318488 | SUPPORT | The clinical aspect and time of onset are generally sufficient to make the correct diagnosis. Nevertheless, peculiar clinical presentations may require additional work-up to rule out life-threatening conditions, and dermatological consultation and histological examination are required for the final diagnosis. | The literature mentions that clinical recognition through observation of typical skin changes can be sufficient for diagnosis, suggesting that a dermatological examination is key in diagnosing Transient Neonatal Pustular Melanosis. |
PMID:33397568 | SUPPORT | An accurate diagnosis is primarily based on the distinct morphologic features of the pustules and the characteristic hyperpigmented macules left behind. | This supports the value of dermatologic examination in diagnosing Transient Neonatal Pustular Melanosis by observing the specific morphologic features. |
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PMID:511427 | SUPPORT | Gram stains of the pustules showed numerous neutrophils but no bacteria. | The use of skin smears in diagnosing transient neonatal pustular melanosis is supported as it reveals neutrophils and an absence of bacteria. |
PMID:9144701 | SUPPORT | The Tzanck smear is a very easy, rapid, and sensitive test for detection of a herpetic infection (multinucleated giant cells) as well as noninfectious pustular eruptions (eosinophils, neutrophils). Therefore the Tzanck smear should be the first test performed. | The statement is supported as the use of skin smears to detect neutrophils in noninfectious pustular eruptions is recommended. |