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<title>Archives of Disease in Childhood - Fetal and Neonatal Edition Images in neonatal medicine</title>
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<title>Archives of Disease in Childhood - Fetal and Neonatal Edition</title>
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<title><![CDATA[Multiple, evolving cutaneous nodules present at birth in a well, term infant]]></title>
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<description><![CDATA[ <p>A term female infant was born weighing 3.4 kg after uneventful antenatal care. There was no significant family medical history of note.</p> <p>Evident at birth were a series of erythematous nodular lesions on the back (10 mm by 10 mm) and groin (8 mm by 8 mm). The nodules were firm and well demarcated, with purple discolouration. There were visible capillaries with an area of central pallor which crusted within 24 hours (<cross-ref type="fig" refid="F1">figure 1</cross-ref>). The rest of the examination was unremarkable. Empirical treatment for infection was given, with a mild C-reactive protein rise to 9 mg/L.</p> <p>A clinical review by dermatology resulted in a punch biopsy of one lesion, and a diagnosis of infantile myofibromatosis was made.</p> <p>Infantile myofibromatosis describes a benign spindle cell tumour of the soft tissues with fibrous proliferation of skin, bone or muscle<cross-ref type="bib" refid="R1">1</cross-ref> and must be present at multiple sites to be diagnostic. It is the most...]]></description>
<dc:creator><![CDATA[Madabhushi, S. R., DSilva, N., King, A.]]></dc:creator>
<dc:date>2026-04-17T00:45:42-07:00</dc:date>
<dc:identifier>info:doi/10.1136/archdischild-2025-329149</dc:identifier>
<dc:identifier>hwp:master-id:fetalneonatal;archdischild-2025-329149</dc:identifier>
<dc:publisher>BMJ Publishing Group</dc:publisher>
<dc:title><![CDATA[Multiple, evolving cutaneous nodules present at birth in a well, term infant]]></dc:title>
<prism:publicationDate>2026-05-01</prism:publicationDate>
<prism:section>Images in neonatal medicine</prism:section>
<prism:volume>111</prism:volume>
<prism:number>3</prism:number>
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<title><![CDATA[Extensive leukaemia cutis at birth]]></title>
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<description><![CDATA[ <sec id="s1"><st>Case</st> <p>A female neonate was delivered at 38 weeks of gestation by emergency caesarean section due to non-reassuring fetal status with polyhydramnios (amniotic fluid index: 39 cm) and fetal hepatomegaly. She presented with hypotonia and poor respiratory effort at birth, requiring intubation and resuscitation. Persistent pulmonary hypertension was diagnosed and treated with 100% oxygen and inhaled nitric oxide. Numerous dark-purple papular to nodular lesions (1&ndash;10 mm) were noted on the face, trunk and extremities, covering nearly the entire body (<cross-ref type="fig" refid="F1">figure 1</cross-ref>). Hepatosplenomegaly was also evident. Laboratory findings included extreme hyperleukocytosis with a leucocyte count of 535.7 <FONT FACE="arial,helvetica">x</FONT> 10<sup>9</sup>/L, anaemia (haemoglobin 7.2 g/dL), a normal platelet count (186 <FONT FACE="arial,helvetica">x</FONT> 10<sup>9</sup>/L), elevated lactate dehydrogenase (7829 IU/L), and hyperuricaemia (uric acid 7.3 mg/dL). Exchange transfusions were performed four times to reduce leukocytosis-related hyperviscosity and manage tumour lysis syndrome. Bone marrow examination showed a predominance of immature monocytic cells, consistent...]]></description>
<dc:creator><![CDATA[Iwatani, S., Ohnishi, Y., Goto, H., Saito, A., Yoshimoto, S.]]></dc:creator>
<dc:date>2026-04-17T00:45:42-07:00</dc:date>
<dc:identifier>info:doi/10.1136/archdischild-2025-329262</dc:identifier>
<dc:identifier>hwp:master-id:fetalneonatal;archdischild-2025-329262</dc:identifier>
<dc:publisher>BMJ Publishing Group</dc:publisher>
<dc:title><![CDATA[Extensive leukaemia cutis at birth]]></dc:title>
<prism:publicationDate>2026-05-01</prism:publicationDate>
<prism:section>Images in neonatal medicine</prism:section>
<prism:volume>111</prism:volume>
<prism:number>3</prism:number>
<prism:startingPage>F285</prism:startingPage>
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