Haematology. Barbara J. Bain. Читать онлайн. Newlib. NEWLIB.NET

Автор: Barbara J. Bain
Издательство: John Wiley & Sons Limited
Серия:
Жанр произведения: Медицина
Год издания: 0
isbn: 9781119777526
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to the above features, some patients sadly develop a treatment‐related myelodysplastic syndrome or acute leukaemia.

      1 Plasmablastic myeloma:Can represent disease evolutionHas a high proliferation index on Ki‐67 stainingHas a worse prognosis than other cases of myelomaIs associated with worse renal function than other cases of myelomaIs associated with a higher serum calcium than other cases of myelomaFor answers and discussion, see page 206.

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      A 5‐year‐old girl was admitted as an emergency after a collapse following a fever at home. On assessment she was acutely unwell and hypotensive and had generalised petechiae. The clinical picture was of severe sepsis and after blood cultures had been taken she was commenced on broad‐spectrum antibiotics. The full blood count showed Hb 120 g/l, WBC 20 × 109/l, neutrophils 17 × 109/l and platelets 32 × 109/l. The coagulation profile was indicative of disseminated intravascular coagulation (DIC). The blood film (left images ×100 objective) showed neutrophilia with left shift; in particular there was prominent neutrophil vacuolation and there were cytoplasmic inclusions consistent with the appearance of diplococci. Note also the prominent Döhle bodies in the neutrophils (bottom left). Meningococcal septicaemia now seemed likely and was confirmed on blood cultures and PCR studies.

      A second patient, a 62‐year‐old man, was admitted following a collapse after a 2‐day prodrome of feeling non‐specifically unwell. He had been bitten on the hand by a dog some days previously. He was febrile and hypotensive and had widespread petechiae. His condition deteriorated and he required intubation, ventilation and inotropic support. His full blood count showed Hb 137 g/l, WBC 24.2 × 109/l, neutrophils 22.7 × 109/l and platelets 9 × 109/l. The coagulation screen was again indicative of DIC (PT 25 s, APTT 92 s, TT 17 s, fibrinogen 1.5 g/l and D dimer 88 726 ng/ml). The blood film showed neutrophilia with left shift and some neutrophils had rod‐shaped bacterial inclusions (centre images). Blood cultures grew the Gram‐negative bacillus, Capnocytophaga canimorsus, which is a serious human pathogen that often forms part of normal canine and feline flora.

      1 Neutrophil vacuolation can be a feature of:Bacterial infectionChédiak–Higashi syndromeEthanol toxicityNeonatal necrotising enterocolitisNeutral lipid storage diseaseFor answers and discussion, see page 206.

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      A 26‐year‐old man was well known to the Haematology clinic and had a chronic compensated haemolytic anaemia due to the unstable haemoglobin, haemoglobin Köln. He suffered exacerbations of haemolysis with intercurrent infection but his condition would settle thereafter. A typical full blood count showed Hb 114 g/l, WBC 4.7 × 109/l, neutrophils 2.4 × 109/l and platelets 154 × 109/l. His blood film is illustrated above; bite cells and irregularly contracted cells are evident (left and centre ×100 objective) and Heinz bodies were prominent (right, methyl violet ×100). Somewhat unexpectedly, he developed progressive and ultimately massive splenomegaly though his haemolytic disorder appeared clinically unchanged. CT scanning showed a 25 cm spleen with no focal abnormality; there was no evidence of chronic liver disease or portal hypertension and no lymphadenopathy was apparent. His full blood count now showed Hb 125 g/l, WBC 12.7 × 109/l, neutrophils 8.9 × 109/l and platelets 1830 × 109/l. He underwent a splenectomy in view of progressive splenic symptoms. The spleen weighed 2700 g (normal 200 g). Histological examination showed massive expansion of the red pulp with congested sinuses and extramedullary haemopoiesis. There was no evidence of lymphoma.

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      The features here support a diagnosis of a myeloproliferative neoplasm and molecular studies showed a pathogenic intragenic CALR deletion. In the circumstances it is difficult to accurately classify this myeloproliferative neoplasm but the diagnosis is likely to be primary myelofibrosis. This patient has two unrelated disorders which had caused understandable diagnostic difficulty. It is important to link any new development to a known disorder but it is also advisable that the clinician keeps an open mind, and considers all potential options when patients show an unexpected clinical evolution.

      1 Unstable haemoglobins:Affect only the α or β globin chainCan be associated with the presence of two variant haemoglobins as well as haemoglobin ACan be detected by instability on heating or exposure to isopropanolHave normal oxygen affinityWhen clinically manifest, usually indicate homozygosityFor answers and discussion, see page 206.

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      A 33‐year‐old woman with known sickle cell anaemia, newly arrived in the United Kingdom, presented to Accident and Emergency with a painful crisis. She was breathless, febrile and faintly jaundiced. Her FBC showed Hb 51 g/l, RBC 1.72 × 1012/l, Hct 0.165, MCV 95.8 fl, MCH 29.8 pg, MCHC 311 g/l, WBC 13.8 × 109/l and platelet count 445 × 109/l. Bilirubin was increased to 141 μmol/l and ALT was mildly increased to 55 u/l. CRP was markedly increased to 137 mg/l. Examination of the blood film (all images ×100 objective) showed boat‐shaped cells (top) but surprisingly infrequent sickle cells. There were some nucleated red blood cells and polychromasia was